HGVS | Genome Assembly |
---|---|
NC_000002.12:g.71124445G= , CM000664.2:g.71124445G= | GRCh38 |
NC_000002.11:g.71351575G= , CM000664.1:g.71351575G= | GRCh37 |
NC_000002.10:g.71205083G= | NCBI36 |
NG_008977.1:g.10820C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000244217.6:c.139C= MANE Select | ENSP00000244217.5:p.Arg47= | |
ENST00000244217.5:c.139C= | ENSP00000244217.5:p.Arg47= | |
ENST00000413592.5:c.7C= | ENSP00000391140.1:p.Arg3= | |
ENST00000486135.1:c.-147C= | ENSP00000441569.1:n.-147C= | |
ENST00000494660.6:c.-147C= | ENSP00000437361.1:n.-147C= | |
NM_032601.3:c.139C= | NP_115990.3:p.Arg47= | |
XM_005264613.2:c.139C= | XP_005264670.1:p.Arg47= | |
XR_939729.1:n.208C= | ||
XR_939729.2:n.208C= | ||
NM_032601.4:c.139C= MANE Select | NP_115990.3:p.Arg47= |