HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240879137T>A , CM000664.2:g.240879137T>A | GRCh38 |
NC_000002.11:g.241818554T>A , CM000664.1:g.241818554T>A | GRCh37 |
NC_000002.10:g.241467227T>A | NCBI36 |
NG_008005.1:g.15393T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.4:c.*316T>A MANE Select | ENSP00000302620.3:n.*316T>A | |
ENST00000470255.1:n.1273T>A | ||
NM_000030.3:c.*316T>A MANE Select | NP_000021.1:n.*316T>A |