HGVS | Genome Assembly |
---|---|
NC_000005.10:g.135028942G>T , CM000667.2:g.135028942G>T | GRCh38 |
NC_000005.9:g.134364632G>T , CM000667.1:g.134364632G>T | GRCh37 |
NC_000005.8:g.134392531G>T | NCBI36 |
NG_012114.1:g.10333C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000265340.12:c.782C>A MANE Select | ENSP00000265340.6:p.Ala261Asp | |
ENST00000265340.11:c.782C>A | ENSP00000265340.6:p.Ala261Asp | |
ENST00000506438.5:c.782C>A | ENSP00000427542.1:p.Ala261Asp | |
NM_002653.4:c.782C>A | NP_002644.4:p.Ala261Asp | |
NM_002653.5:c.782C>A MANE Select | NP_002644.4:p.Ala261Asp |