HGVS | Genome Assembly |
---|---|
NC_000001.11:g.172665707T>G , CM000663.2:g.172665707T>G | GRCh38 |
NC_000001.10:g.172634847T>G , CM000663.1:g.172634847T>G | GRCh37 |
NC_000001.9:g.170901470T>G | NCBI36 |
NG_007269.1:g.11663T>G , LRG_58:g.11663T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367721.3:c.537T>G MANE Select | ENSP00000356694.2:p.Gly179= | |
ENST00000340030.4:c.*107T>G | ENSP00000344739.3:n.*107T>G | |
ENST00000367721.2:c.537T>G | ENSP00000356694.2:p.Gly179= | |
NM_000639.2:c.537T>G | NP_000630.1:p.Gly179= | |
NM_001302746.1:c.*107T>G | NP_001289675.1:n.*107T>G | |
NM_000639.3:c.537T>G MANE Select | NP_000630.1:p.Gly179= | |
NM_001302746.2:c.*107T>G | NP_001289675.1:n.*107T>G |