HGVS | Genome Assembly |
---|---|
NC_000003.12:g.190388182A>C , CM000665.2:g.190388182A>C | GRCh38 |
NC_000003.11:g.190105971A>C , CM000665.1:g.190105971A>C | GRCh37 |
NC_000003.10:g.191588665A>C | NCBI36 |
NG_008149.1:g.5131A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264734.3:c.-148A>C MANE Select | ENSP00000264734.3:n.-148A>C | |
ENST00000456423.2:c.-148A>C | ENSP00000414136.2:n.-148A>C | |
ENST00000264734.2:c.63A>C | ENSP00000264734.2:p.Arg21Ser | |
ENST00000456423.1:c.63A>C | ENSP00000414136.1:p.Arg21Ser | |
ENST00000468220.1:n.306+13579A>C | ||
NM_006580.3:c.63A>C | NP_006571.1:p.Arg21Ser | |
NM_001378492.1:c.-93-55A>C | NP_001365421.1:n.-93-55A>C | |
NM_001378493.1:c.-93-55A>C | NP_001365422.1:n.-93-55A>C | |
NM_006580.4:c.-148A>C MANE Select | NP_006571.2:n.-148A>C |