Linked Data
ClinVar Variation Id:
892522
ClinVar RCV Id:
RCV001128621
dbSNP Id:
rs2071338251
gnomAD v4:
17-7223676-C-T
MyVariant Identifiers:
chr17:g.7126995C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7223676C>T , CM000679.2:g.7223676C>T | GRCh38 |
| NC_000017.10:g.7126995C>T , CM000679.1:g.7126995C>T | GRCh37 |
| NC_000017.9:g.7067719C>T | NCBI36 |
| NG_007975.1:g.8843C>T | |
| NG_008391.2:g.1375G>A | |
| NG_033038.1:g.15869G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356839.10:c.1215C>T MANE Select | ENSP00000349297.5:p.Asp405= | |
| ENST00000322910.9:c.*1170C>T | ENSP00000325395.5:n.*1170C>T | |
| ENST00000350303.9:c.1149C>T | ENSP00000344152.5:p.Asp383= | |
| ENST00000356839.9:c.1215C>T | ENSP00000349297.5:p.Asp405= | |
| ENST00000542255.6:c.73C>T | ||
| ENST00000543245.6:c.1284C>T | ENSP00000438689.2:p.Asp428= | |
| ENST00000578579.2:n.386C>T | ||
| ENST00000578711.1:n.172C>T | ||
| ENST00000578824.5:n.631C>T | ||
| ENST00000579425.5:n.239C>T | ||
| ENST00000579546.1:c.52C>T | ||
| ENST00000583858.5:c.244C>T | ||
| ENST00000585203.6:n.423C>T | ||
| NM_000018.3:c.1215C>T | NP_000009.1:p.Asp405= | |
| NM_001033859.2:c.1149C>T | NP_001029031.1:p.Asp383= | |
| NM_001270447.1:c.1284C>T | NP_001257376.1:p.Asp428= | |
| NM_001270448.1:c.987C>T | NP_001257377.1:p.Asp329= | |
| XM_006721516.2:c.1215C>T | XP_006721579.2:p.Asp405= | |
| XM_011523829.1:c.1215C>T | XP_011522131.1:p.Asp405= | |
| XM_011523830.1:c.1215C>T | XP_011522132.1:p.Asp405= | |
| XR_934021.1:n.1322C>T | ||
| XR_934022.1:n.1322C>T | ||
| XR_934023.1:n.1322C>T | ||
| XM_006721516.3:c.1215C>T | XP_006721579.2:p.Asp405= | |
| XM_011523829.2:c.1215C>T | XP_011522131.1:p.Asp405= | |
| XM_011523830.2:c.1215C>T | XP_011522132.1:p.Asp405= | |
| XM_024450741.1:c.1215C>T | XP_024306509.1:p.Asp405= | |
| XR_934021.2:n.1274C>T | ||
| XR_934022.2:n.1274C>T | ||
| XR_934023.2:n.1274C>T | ||
| NM_000018.4:c.1215C>T MANE Select | NP_000009.1:p.Asp405= | |
| NM_001033859.3:c.1149C>T | NP_001029031.1:p.Asp383= | |
| NM_001270447.2:c.1284C>T | NP_001257376.1:p.Asp428= | |
| NM_001270448.2:c.987C>T | NP_001257377.1:p.Asp329= |