Linked Data
dbSNP Id:
rs1732599576
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.156971701C>A , CM000666.2:g.156971701C>A | GRCh38 |
| NC_000004.11:g.157892853C>A , CM000666.1:g.157892853C>A | GRCh37 |
| NC_000004.10:g.158112303C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502773.6:c.-798G>T MANE Select | ENSP00000422464.1:n.-798G>T | |
| NM_016205.3:c.-798G>T MANE Select | NP_057289.1:n.-798G>T | |
| NR_036641.2:n.99G>T |