HGVS | Genome Assembly |
---|---|
NC_000006.12:g.35805943T>A , CM000668.2:g.35805943T>A | GRCh38 |
NC_000006.11:g.35773720T>A , CM000668.1:g.35773720T>A | GRCh37 |
NC_000006.10:g.35881698T>A | NCBI36 |
NG_012184.1:g.5650T>A | |
NG_012184.2:g.5650T>A | |
NG_012184.3:g.13738T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360215.3:c.273T>A MANE Select | ENSP00000353346.1:p.Ser91= | |
ENST00000651132.1:c.273T>A | ENSP00000498322.1:p.Ser91= | |
ENST00000651676.1:c.273T>A | ENSP00000498699.1:p.Ser91= | |
ENST00000651994.1:c.273T>A | ENSP00000498310.1:p.Ser91= | |
ENST00000652718.1:c.105T>A | ENSP00000498866.1:p.Ser35= | |
ENST00000360215.2:c.273T>A | ENSP00000353346.1:p.Ser91= | |
NM_182548.3:c.273T>A | NP_872354.1:p.Ser91= | |
XM_011514403.1:c.273T>A | XP_011512705.1:p.Ser91= | |
NM_182548.4:c.273T>A MANE Select | NP_872354.1:p.Ser91= |