Linked Data
dbSNP Id:
rs1667614339
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.101421511G>A , CM000671.2:g.101421511G>A | GRCh38 |
| NC_000009.11:g.104183793G>A , CM000671.1:g.104183793G>A | GRCh37 |
| NC_000009.10:g.103223614G>A | NCBI36 |
| NG_012387.1:g.19270C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647789.2:c.*298C>T MANE Select | ENSP00000497767.1:n.*298C>T | |
| ENST00000648064.1:c.*298C>T | ENSP00000497990.1:n.*298C>T | |
| ENST00000374855.8:c.*298C>T | ENSP00000363988.4:n.*298C>T | |
| NM_000035.3:c.*298C>T | NP_000026.2:n.*298C>T | |
| NM_000035.4:c.*298C>T MANE Select | NP_000026.2:n.*298C>T |