Linked Data
dbSNP Id:
rs1721010655
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55125492G>A , CM000666.2:g.55125492G>A | GRCh38 |
| NC_000004.11:g.55991659G>A , CM000666.1:g.55991659G>A | GRCh37 |
| NC_000004.10:g.55686416G>A | NCBI36 |
| NG_012004.1:g.5104C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263923.5:c.-199C>T MANE Select | ENSP00000263923.4:n.-199C>T | |
| ENST00000263923.4:c.-199C>T | ENSP00000263923.4:n.-199C>T | |
| NM_002253.2:c.-199C>T | NP_002244.1:n.-199C>T | |
| NM_002253.3:c.-199C>T | NP_002244.1:n.-199C>T | |
| NM_002253.4:c.-199C>T MANE Select | NP_002244.1:n.-199C>T |