HGVS | Genome Assembly |
---|---|
NC_000005.10:g.135028853G>A , CM000667.2:g.135028853G>A | GRCh38 |
NC_000005.9:g.134364543G>A , CM000667.1:g.134364543G>A | GRCh37 |
NC_000005.8:g.134392442G>A | NCBI36 |
NG_012114.1:g.10422C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000265340.12:c.871C>T MANE Select | ENSP00000265340.6:p.Gln291Ter | |
ENST00000265340.11:c.871C>T | ENSP00000265340.6:p.Gln291Ter | |
ENST00000506438.5:c.871C>T | ENSP00000427542.1:p.Gln291Ter | |
NM_002653.4:c.871C>T | NP_002644.4:p.Gln291Ter | |
NM_002653.5:c.871C>T MANE Select | NP_002644.4:p.Gln291Ter |