HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73332260G>A , CM000677.2:g.73332260G>A | GRCh38 |
NC_000015.9:g.73624601G>A , CM000677.1:g.73624601G>A | GRCh37 |
NC_000015.8:g.71411654G>A | NCBI36 |
NG_009063.1:g.42005C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261917.4:c.1242C>T MANE Select | ENSP00000261917.3:p.Ala414= | |
ENST00000261917.3:c.1242C>T | ENSP00000261917.3:p.Ala414= | |
NM_005477.2:c.1242C>T | NP_005468.1:p.Ala414= | |
XM_011521148.1:c.24C>T | XP_011519450.1:p.Ala8= | |
XM_011521148.2:c.24C>T | XP_011519450.1:p.Ala8= | |
NM_005477.3:c.1242C>T MANE Select | NP_005468.1:p.Ala414= |