Linked Data
ClinVar Variation Id:
2886960
ClinVar RCV Id:
RCV003750498
dbSNP Id:
rs200385894
ExAC:
X:153132191 C / T
gnomAD v2:
X-153132191-C-T
gnomAD v3:
X-153866736-C-T
gnomAD v4:
X-153866736-C-T
COSMIC:
COSM4107906
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153866736C>T , CM000685.2:g.153866736C>T | GRCh38 |
| NC_000023.10:g.153132191C>T , CM000685.1:g.153132191C>T | GRCh37 |
| NC_000023.9:g.152785385C>T | NCBI36 |
| NG_009645.3:g.47488G>A | |
| NG_009645.4:g.24438G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370060.7:c.2344G>A MANE Select | ENSP00000359077.1:p.Val782Met | |
| ENST00000361699.8:c.2344G>A | ENSP00000355380.4:p.Val782Met | |
| ENST00000361981.7:c.2329G>A | ENSP00000354712.3:p.Val777Met | |
| ENST00000370055.5:c.2329G>A | ENSP00000359072.1:p.Val777Met | |
| ENST00000370060.5:c.2344G>A | ENSP00000359077.1:p.Val782Met | |
| NM_000425.4:c.2344G>A | NP_000416.1:p.Val782Met | |
| NM_001143963.2:c.2329G>A | NP_001137435.1:p.Val777Met | |
| NM_001278116.1:c.2344G>A | NP_001265045.1:p.Val782Met | |
| NM_024003.3:c.2344G>A | NP_076493.1:p.Val782Met | |
| NM_000425.5:c.2344G>A | NP_000416.1:p.Val782Met | |
| NM_001278116.2:c.2344G>A MANE Select | NP_001265045.1:p.Val782Met |