Linked Data
ClinVar Variation Id:
1533564
ClinVar RCV Id:
RCV002082480
dbSNP Id:
rs2142985123
MyVariant Identifiers:
chr17:g.7127170C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7223851C>A , CM000679.2:g.7223851C>A | GRCh38 |
| NC_000017.10:g.7127170C>A , CM000679.1:g.7127170C>A | GRCh37 |
| NC_000017.9:g.7067894C>A | NCBI36 |
| NG_007975.1:g.9018C>A | |
| NG_008391.2:g.1200G>T | |
| NG_033038.1:g.15694G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356839.10:c.1308C>A MANE Select | ENSP00000349297.5:p.Ile436= | |
| ENST00000322910.9:c.*1263C>A | ENSP00000325395.5:n.*1263C>A | |
| ENST00000350303.9:c.1242C>A | ENSP00000344152.5:p.Ile414= | |
| ENST00000356839.9:c.1308C>A | ENSP00000349297.5:p.Ile436= | |
| ENST00000542255.6:c.166C>A | ||
| ENST00000543245.6:c.1377C>A | ENSP00000438689.2:p.Ile459= | |
| ENST00000578711.1:n.347C>A | ||
| ENST00000579425.5:n.332C>A | ||
| ENST00000579546.1:c.145C>A | ||
| ENST00000583074.5:n.27C>A | ||
| ENST00000583850.5:n.83C>A | ||
| ENST00000583858.5:c.337C>A | ||
| ENST00000585203.6:n.516C>A | ||
| NM_000018.3:c.1308C>A | NP_000009.1:p.Ile436= | |
| NM_001033859.2:c.1242C>A | NP_001029031.1:p.Ile414= | |
| NM_001270447.1:c.1377C>A | NP_001257376.1:p.Ile459= | |
| NM_001270448.1:c.1080C>A | NP_001257377.1:p.Ile360= | |
| XM_006721516.2:c.1308C>A | XP_006721579.2:p.Ile436= | |
| XM_011523829.1:c.1308C>A | XP_011522131.1:p.Ile436= | |
| XM_011523830.1:c.1308C>A | XP_011522132.1:p.Ile436= | |
| XR_934021.1:n.1415C>A | ||
| XR_934022.1:n.1415C>A | ||
| XR_934023.1:n.1415C>A | ||
| XM_006721516.3:c.1308C>A | XP_006721579.2:p.Ile436= | |
| XM_011523829.2:c.1308C>A | XP_011522131.1:p.Ile436= | |
| XM_011523830.2:c.1308C>A | XP_011522132.1:p.Ile436= | |
| XM_024450741.1:c.1308C>A | XP_024306509.1:p.Ile436= | |
| XR_934021.2:n.1367C>A | ||
| XR_934022.2:n.1367C>A | ||
| XR_934023.2:n.1367C>A | ||
| NM_000018.4:c.1308C>A MANE Select | NP_000009.1:p.Ile436= | |
| NM_001033859.3:c.1242C>A | NP_001029031.1:p.Ile414= | |
| NM_001270447.2:c.1377C>A | NP_001257376.1:p.Ile459= | |
| NM_001270448.2:c.1080C>A | NP_001257377.1:p.Ile360= |