Canonical Allele Identifier: CA1403197703
Gene: SLCO2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133948892C= , CM000665.2:g.133948892C= GRCh38
NC_000003.11:g.133667736C= , CM000665.1:g.133667736C= GRCh37
NC_000003.10:g.135150426C= NCBI36
NG_031964.2:g.108293G=
NG_031964.3:g.108293G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310926.11:c.940+1G= MANE Select ENSP00000311291.4:n.940+1G=
ENST00000310926.8:c.940+1G= ENSP00000311291.4:n.940+1G=
ENST00000462770.5:n.521-192G=
ENST00000477061.1:n.324+1G=
ENST00000481359.3:c.940+1G= ENSP00000420028.3:n.940+1G=
ENST00000493729.5:c.712+1G= ENSP00000418893.1:n.712+1G=
NM_005630.2:c.940+1G= NP_005621.2:n.940+1G=
XM_011513090.1:c.940+1G= XP_011511392.1:n.940+1G=
XM_017007077.1:c.436+1G= XP_016862566.1:n.436+1G=
XM_024453721.1:c.940+1G= XP_024309489.1:n.940+1G=
NM_005630.3:c.940+1G= MANE Select NP_005621.2:n.940+1G=