Linked Data
dbSNP Id:
rs201429392
ExAC:
11:64517799 C / T
gnomAD v2:
11-64517799-C-T
gnomAD v3:
11-64750327-C-T
gnomAD v4:
11-64750327-C-T
COSMIC:
COSN5264060
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.64750327C>T , CM000673.2:g.64750327C>T | GRCh38 |
| NC_000011.9:g.64517799C>T , CM000673.1:g.64517799C>T | GRCh37 |
| NC_000011.8:g.64274375C>T | NCBI36 |
| NG_007574.1:g.130G>A , LRG_100:g.130G>A | |
| NG_013018.1:g.15389G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000164139.4:c.2177+49G>A MANE Select | ENSP00000164139.3:n.2177+49G>A | |
| ENST00000164139.3:c.2177+49G>A | ENSP00000164139.3:n.2177+49G>A | |
| ENST00000377432.7:c.1913+49G>A | ENSP00000366650.3:n.1913+49G>A | |
| NM_001164716.1:c.1913+49G>A | NP_001158188.1:n.1913+49G>A | |
| NM_005609.2:c.2177+49G>A | NP_005600.1:n.2177+49G>A | |
| NM_005609.3:c.2177+49G>A | NP_005600.1:n.2177+49G>A | |
| NM_005609.4:c.2177+49G>A MANE Select | NP_005600.1:n.2177+49G>A |