Canonical Allele Identifier: CA1403200187
Gene: SLCO2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133951305C= , CM000665.2:g.133951305C= GRCh38
NC_000003.11:g.133670149C= , CM000665.1:g.133670149C= GRCh37
NC_000003.10:g.135152839C= NCBI36
NG_031964.2:g.105880G=
NG_031964.3:g.105880G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310926.11:c.764G= MANE Select ENSP00000311291.4:p.Gly255=
ENST00000310926.8:c.764G= ENSP00000311291.4:p.Gly255=
ENST00000462770.5:n.521-2605G=
ENST00000464676.5:n.1026G=
ENST00000481359.3:c.764G= ENSP00000420028.3:p.Gly255=
ENST00000493729.5:c.536G= ENSP00000418893.1:p.Gly179=
NM_005630.2:c.764G= NP_005621.2:p.Gly255=
XM_011513090.1:c.764G= XP_011511392.1:p.Gly255=
XM_017007077.1:c.260G= XP_016862566.1:p.Gly87=
XM_024453721.1:c.764G= XP_024309489.1:p.Gly255=
NM_005630.3:c.764G= MANE Select NP_005621.2:p.Gly255=