HGVS | Genome Assembly |
---|---|
NC_000008.11:g.18400754G= , CM000670.2:g.18400754G= | GRCh38 |
NC_000008.10:g.18258264G= , CM000670.1:g.18258264G= | GRCh37 |
NC_000008.9:g.18302544G= | NCBI36 |
NG_012246.1:g.14510G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286479.4:c.751G= MANE Select | ENSP00000286479.3:p.Asp251= | |
ENST00000286479.3:c.751G= | ENSP00000286479.3:p.Asp251= | |
ENST00000520116.1:c.361G= | ENSP00000428416.1:p.Asp121= | |
NM_000015.2:c.751G= | NP_000006.2:p.Asp251= | |
XM_011544358.1:c.751G= | XP_011542660.1:p.Asp251= | |
XM_017012938.1:c.751G= | XP_016868427.1:p.Asp251= | |
NM_000015.3:c.751G= MANE Select | NP_000006.2:p.Asp251= |