Linked Data
dbSNP Id:
rs2124494923
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.40097399C>T , CM000663.2:g.40097399C>T | GRCh38 |
| NC_000001.10:g.40563071C>T , CM000663.1:g.40563071C>T | GRCh37 |
| NC_000001.9:g.40335658C>T | NCBI36 |
| NG_009192.1:g.5072G>A , LRG_690:g.5072G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000433473.7:c.-161G>A | ENSP00000394863.3:n.-161G>A | |
| NM_000310.3:c.-161G>A , LRG_690t1:c.-161G>A | NP_000301.1:n.-161G>A | |
| NM_001142604.1:c.-161G>A | NP_001136076.1:n.-161G>A | |
| NM_001363695.1:c.-161G>A | NP_001350624.1:n.-161G>A |