Linked Data
ClinVar Variation Id:
854698
ClinVar RCV Id:
RCV001059797
dbSNP Id:
rs1197133430
gnomAD v4:
17-7222197-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7222197T>C , CM000679.2:g.7222197T>C | GRCh38 |
| NC_000017.10:g.7125516T>C , CM000679.1:g.7125516T>C | GRCh37 |
| NC_000017.9:g.7066240T>C | NCBI36 |
| NG_007975.1:g.7364T>C | |
| NG_008391.2:g.2854A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356839.10:c.773T>C MANE Select | ENSP00000349297.5:p.Ile258Thr | |
| ENST00000322910.9:c.*728T>C | ENSP00000325395.5:n.*728T>C | |
| ENST00000350303.9:c.707T>C | ENSP00000344152.5:p.Ile236Thr | |
| ENST00000356839.9:c.773T>C | ENSP00000349297.5:p.Ile258Thr | |
| ENST00000543245.6:c.842T>C | ENSP00000438689.2:p.Ile281Thr | |
| ENST00000577191.5:n.945T>C | ||
| ENST00000581378.5:c.491T>C | ||
| ENST00000582379.1:n.157T>C | ||
| NM_000018.3:c.773T>C | NP_000009.1:p.Ile258Thr | |
| NM_001033859.2:c.707T>C | NP_001029031.1:p.Ile236Thr | |
| NM_001270447.1:c.842T>C | NP_001257376.1:p.Ile281Thr | |
| NM_001270448.1:c.545T>C | NP_001257377.1:p.Ile182Thr | |
| XM_006721516.2:c.773T>C | XP_006721579.2:p.Ile258Thr | |
| XM_011523829.1:c.773T>C | XP_011522131.1:p.Ile258Thr | |
| XM_011523830.1:c.773T>C | XP_011522132.1:p.Ile258Thr | |
| XR_934021.1:n.880T>C | ||
| XR_934022.1:n.880T>C | ||
| XR_934023.1:n.880T>C | ||
| XM_006721516.3:c.773T>C | XP_006721579.2:p.Ile258Thr | |
| XM_011523829.2:c.773T>C | XP_011522131.1:p.Ile258Thr | |
| XM_011523830.2:c.773T>C | XP_011522132.1:p.Ile258Thr | |
| XM_024450741.1:c.773T>C | XP_024306509.1:p.Ile258Thr | |
| XR_934021.2:n.832T>C | ||
| XR_934022.2:n.832T>C | ||
| XR_934023.2:n.832T>C | ||
| NM_000018.4:c.773T>C MANE Select | NP_000009.1:p.Ile258Thr | |
| NM_001033859.3:c.707T>C | NP_001029031.1:p.Ile236Thr | |
| NM_001270447.2:c.842T>C | NP_001257376.1:p.Ile281Thr | |
| NM_001270448.2:c.545T>C | NP_001257377.1:p.Ile182Thr |