HGVS | Genome Assembly |
---|---|
NC_000008.11:g.96145178T>A , CM000670.2:g.96145178T>A | GRCh38 |
NC_000008.10:g.97157406T>A , CM000670.1:g.97157406T>A | GRCh37 |
NC_000008.9:g.97226582T>A | NCBI36 |
NG_008981.1:g.20615A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000287020.7:c.753A>T MANE Select | ENSP00000287020.4:p.Gly251= | |
ENST00000287020.6:c.753A>T | ENSP00000287020.4:p.Gly251= | |
ENST00000620978.1:c.707-16A>T | ENSP00000480170.1:n.707-16A>T | |
ENST00000621429.1:c.753A>T | ENSP00000483711.1:p.Gly251= | |
NM_001001557.2:c.753A>T | NP_001001557.1:p.Gly251= | |
XM_011517030.1:c.354A>T | XP_011515332.1:p.Gly118= | |
NM_001001557.3:c.753A>T | NP_001001557.1:p.Gly251= | |
NM_001001557.4:c.753A>T MANE Select | NP_001001557.1:p.Gly251= |