HGVS | Genome Assembly |
---|---|
NC_000001.11:g.53196813G>T , CM000663.2:g.53196813G>T | GRCh38 |
NC_000001.10:g.53662485G>T , CM000663.1:g.53662485G>T | GRCh37 |
NC_000001.9:g.53435073G>T | NCBI36 |
NG_008035.1:g.5385G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000636239.1:c.-131G>T | ENSP00000490066.1:n.-131G>T | |
ENST00000636867.1:c.-131G>T | ENSP00000489631.1:n.-131G>T | |
ENST00000636891.1:c.-131G>T | ENSP00000490399.1:n.-131G>T | |
ENST00000636935.1:c.-131G>T | ENSP00000489757.1:n.-131G>T | |
ENST00000637252.1:c.-131G>T | ENSP00000490492.1:n.-131G>T | |
ENST00000371486.3:c.-131G>T | ENSP00000360541.3:n.-131G>T | |
NM_000098.2:c.-131G>T | NP_000089.1:n.-131G>T | |
XM_005270484.1:c.-131G>T | XP_005270541.1:n.-131G>T | |
NM_001330589.1:c.-131G>T | NP_001317518.1:n.-131G>T |