Linked Data
ClinVar Variation Id:
55858
dbSNP Id:
rs371707778
ExAC:
9:95480229 G / A
gnomAD v2:
9-95480229-G-A
gnomAD v3:
9-92717947-G-A
gnomAD v4:
9-92717947-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.92717947G>A , CM000671.2:g.92717947G>A | GRCh38 |
| NC_000009.11:g.95480229G>A , CM000671.1:g.95480229G>A | GRCh37 |
| NC_000009.10:g.94520050G>A | NCBI36 |
| NG_033908.1:g.51855C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356884.11:c.2108C>T MANE Select | ENSP00000349351.6:p.Thr703Met | |
| ENST00000356884.10:c.2108C>T | ENSP00000349351.6:p.Thr703Met | |
| ENST00000375512.3:c.2108C>T | ENSP00000364662.3:p.Thr703Met | |
| NM_001003800.1:c.2108C>T | NP_001003800.1:p.Thr703Met | |
| NM_015250.3:c.2108C>T | NP_056065.1:p.Thr703Met | |
| XM_017014551.1:c.2189C>T | XP_016870040.1:p.Thr730Met | |
| NM_001003800.2:c.2108C>T MANE Select | NP_001003800.1:p.Thr703Met | |
| NM_015250.4:c.2108C>T | NP_056065.1:p.Thr703Met |