HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154953942G>A , CM000685.2:g.154953942G>A | GRCh38 |
NC_000023.10:g.154182217G>A , CM000685.1:g.154182217G>A | GRCh37 |
NC_000023.9:g.153835411G>A | NCBI36 |
NG_011403.1:g.73782C>T | |
NG_011403.2:g.73782C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.1853C>T MANE Select | ENSP00000353393.4:p.Ala618Val | |
ENST00000647125.1:c.*1729C>T | ENSP00000496062.1:n.*1729C>T | |
ENST00000360256.8:c.1853C>T | ENSP00000353393.4:p.Ala618Val | |
NM_000132.3:c.1853C>T | NP_000123.1:p.Ala618Val | |
XM_011531126.1:c.1748C>T | XP_011529428.1:p.Ala583Val | |
NM_000132.4:c.1853C>T MANE Select | NP_000123.1:p.Ala618Val |