Canonical Allele Identifier: CA2626556
Community Standard Title: NM_005630.3(SLCO2A1):c.1106G>A (p.Gly369Asp)
Gene: SLCO2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133947445C>T , CM000665.2:g.133947445C>T GRCh38
NC_000003.11:g.133666289C>T , CM000665.1:g.133666289C>T GRCh37
NC_000003.10:g.135148979C>T NCBI36
NG_031964.2:g.109740G>A
NG_031964.3:g.109740G>A

Transcript Alleles

HGVS Amino-acid Change
NM_005630.3:c.1106G>A MANE Select NP_005621.2:p.Gly369Asp
ENST00000310926.11:c.1106G>A MANE Select ENSP00000311291.4:p.Gly369Asp
NM_005630.2:c.1106G>A NP_005621.2:p.Gly369Asp
ENST00000310926.8:c.1106G>A ENSP00000311291.4:p.Gly369Asp
ENST00000462770.5:n.686G>A
ENST00000481359.3:c.1105+1091G>A ENSP00000420028.3:n.1105+1091G>A
ENST00000493729.5:c.878G>A ENSP00000418893.1:p.Gly293Asp
XM_011513090.1:c.1106G>A XP_011511392.1:p.Gly369Asp
XM_017007077.1:c.602G>A XP_016862566.1:p.Gly201Asp
XM_024453721.1:c.1106G>A XP_024309489.1:p.Gly369Asp