HGVS | Genome Assembly |
---|---|
NC_000006.12:g.35805914G>A , CM000668.2:g.35805914G>A | GRCh38 |
NC_000006.11:g.35773691G>A , CM000668.1:g.35773691G>A | GRCh37 |
NC_000006.10:g.35881669G>A | NCBI36 |
NG_012184.1:g.5621G>A | |
NG_012184.2:g.5621G>A | |
NG_012184.3:g.13709G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360215.3:c.244G>A MANE Select | ENSP00000353346.1:p.Gly82Ser | |
ENST00000651132.1:c.244G>A | ENSP00000498322.1:p.Gly82Ser | |
ENST00000651676.1:c.244G>A | ENSP00000498699.1:p.Gly82Ser | |
ENST00000651994.1:c.244G>A | ENSP00000498310.1:p.Gly82Ser | |
ENST00000652718.1:c.76G>A | ENSP00000498866.1:p.Gly26Ser | |
ENST00000360215.2:c.244G>A | ENSP00000353346.1:p.Gly82Ser | |
NM_182548.3:c.244G>A | NP_872354.1:p.Gly82Ser | |
XM_011514403.1:c.244G>A | XP_011512705.1:p.Gly82Ser | |
NM_182548.4:c.244G>A MANE Select | NP_872354.1:p.Gly82Ser |