Linked Data
dbSNP Id:
rs139297964
ExAC:
8:11405575 C / T
gnomAD v2:
8-11405575-C-T
gnomAD v3:
8-11548066-C-T
gnomAD v4:
8-11548066-C-T
COSMIC:
COSM1095173
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.11548066C>T , CM000670.2:g.11548066C>T | GRCh38 |
| NC_000008.10:g.11405575C>T , CM000670.1:g.11405575C>T | GRCh37 |
| NC_000008.9:g.11442984C>T | NCBI36 |
| NG_023543.1:g.59055C>T | |
| NG_023543.2:g.59055C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696154.2:n.361C>T | ||
| ENST00000696154.1:c.-4C>T | ENSP00000512445.1:n.-4C>T | |
| ENST00000259089.9:c.210C>T MANE Select | ENSP00000259089.4:p.Thr70= | |
| ENST00000645242.1:c.-4C>T | ENSP00000494690.1:n.-4C>T | |
| ENST00000259089.8:c.210C>T | ENSP00000259089.4:p.Thr70= | |
| ENST00000529894.1:c.-4C>T | ENSP00000433663.1:n.-4C>T | |
| ENST00000533828.1:n.408C>T | ||
| NM_001715.2:c.210C>T | NP_001706.2:p.Thr70= | |
| XM_011543824.1:c.210C>T | XP_011542126.1:p.Thr70= | |
| XM_011543825.1:c.210C>T | XP_011542127.1:p.Thr70= | |
| XM_011543826.1:c.210C>T | XP_011542128.1:p.Thr70= | |
| XM_011543827.1:c.-4C>T | XP_011542129.1:n.-4C>T | |
| XM_011543828.1:c.210C>T | XP_011542130.1:p.Thr70= | |
| XM_011543829.1:c.210C>T | XP_011542131.1:p.Thr70= | |
| NM_001330465.1:c.-4C>T | NP_001317394.1:n.-4C>T | |
| XM_011543825.3:c.210C>T | XP_011542127.1:p.Thr70= | |
| XM_011543828.3:c.210C>T | XP_011542130.1:p.Thr70= | |
| XM_011543829.3:c.210C>T | XP_011542131.1:p.Thr70= | |
| NM_001715.3:c.210C>T MANE Select | NP_001706.2:p.Thr70= | |
| NM_001330465.2:c.-4C>T | NP_001317394.1:n.-4C>T |