Linked Data
dbSNP Id:
rs1578611920
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.119320473A>T , CM000666.2:g.119320473A>T | GRCh38 |
| NC_000004.11:g.120241628A>T , CM000666.1:g.120241628A>T | GRCh37 |
| NC_000004.10:g.120461076A>T | NCBI36 |
| NG_011444.1:g.6689T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274024.4:c.240+197T>A MANE Select | ENSP00000274024.3:n.240+197T>A | |
| ENST00000274024.3:c.240+197T>A | ENSP00000274024.3:n.240+197T>A | |
| NM_000134.3:c.240+197T>A | NP_000125.2:n.240+197T>A | |
| NM_000134.4:c.240+197T>A MANE Select | NP_000125.2:n.240+197T>A |