HGVS | Genome Assembly |
---|---|
NC_000008.11:g.42732535C>G , CM000670.2:g.42732535C>G | GRCh38 |
NC_000008.10:g.42587678C>G , CM000670.1:g.42587678C>G | GRCh37 |
NC_000008.9:g.42706835C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000289957.3:c.1228C>G MANE Select | ENSP00000289957.2:p.His410Asp | |
ENST00000289957.2:c.1228C>G | ENSP00000289957.2:p.His410Asp | |
NM_000749.3:c.1228C>G | NP_000740.1:p.His410Asp | |
XM_011544390.1:c.841C>G | XP_011542692.1:p.His281Asp | |
NM_000749.4:c.1228C>G | NP_000740.1:p.His410Asp | |
NM_001347717.1:c.1006C>G | NP_001334646.1:p.His336Asp | |
XM_011544390.2:c.841C>G | XP_011542692.1:p.His281Asp | |
NM_000749.5:c.1228C>G MANE Select | NP_000740.1:p.His410Asp | |
NM_001347717.2:c.1006C>G | NP_001334646.1:p.His336Asp |