Linked Data
ClinVar Variation Id:
310196
ClinVar RCV Id:
RCV000338691
dbSNP Id:
rs141736156
gnomAD v3:
12-64716316-C-T
gnomAD v4:
12-64716316-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.64716316C>T , CM000674.2:g.64716316C>T | GRCh38 |
| NC_000012.11:g.65110096C>T , CM000674.1:g.65110096C>T | GRCh37 |
| NC_000012.10:g.63396363C>T | NCBI36 |
| NG_008955.1:g.48131G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258145.8:c.*425G>A MANE Select | ENSP00000258145.3:n.*425G>A | |
| ENST00000258145.7:c.*425G>A | ENSP00000258145.3:n.*425G>A | |
| ENST00000418919.6:c.*425G>A | ENSP00000413130.2:n.*425G>A | |
| NM_002076.3:c.*425G>A | NP_002067.1:n.*425G>A | |
| NM_002076.4:c.*425G>A MANE Select | NP_002067.1:n.*425G>A |