HGVS | Genome Assembly |
---|---|
NC_000003.12:g.190388180A>G , CM000665.2:g.190388180A>G | GRCh38 |
NC_000003.11:g.190105969A>G , CM000665.1:g.190105969A>G | GRCh37 |
NC_000003.10:g.191588663A>G | NCBI36 |
NG_008149.1:g.5129A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264734.3:c.-150A>G MANE Select | ENSP00000264734.3:n.-150A>G | |
ENST00000456423.2:c.-150A>G | ENSP00000414136.2:n.-150A>G | |
ENST00000264734.2:c.61A>G | ENSP00000264734.2:p.Arg21Gly | |
ENST00000456423.1:c.61A>G | ENSP00000414136.1:p.Arg21Gly | |
ENST00000468220.1:n.306+13577A>G | ||
NM_006580.3:c.61A>G | NP_006571.1:p.Arg21Gly | |
NM_001378492.1:c.-93-57A>G | NP_001365421.1:n.-93-57A>G | |
NM_001378493.1:c.-93-57A>G | NP_001365422.1:n.-93-57A>G | |
NM_006580.4:c.-150A>G MANE Select | NP_006571.2:n.-150A>G |