HGVS | Genome Assembly |
---|---|
NC_000001.11:g.40097429T>C , CM000663.2:g.40097429T>C | GRCh38 |
NC_000001.10:g.40563101T>C , CM000663.1:g.40563101T>C | GRCh37 |
NC_000001.9:g.40335688T>C | NCBI36 |
NG_009192.1:g.5042A>G , LRG_690:g.5042A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000433473.7:c.-191A>G | ENSP00000394863.3:n.-191A>G | |
NM_000310.3:c.-191A>G , LRG_690t1:c.-191A>G | NP_000301.1:n.-191A>G | |
NM_001142604.1:c.-191A>G | NP_001136076.1:n.-191A>G | |
NM_001363695.1:c.-191A>G | NP_001350624.1:n.-191A>G |