Canonical Allele Identifier: CA2626851
Gene: SLCO2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133973653A>G , CM000665.2:g.133973653A>G GRCh38
NC_000003.11:g.133692497A>G , CM000665.1:g.133692497A>G GRCh37
NC_000003.10:g.135175187A>G NCBI36
NG_031964.2:g.83532T>C
NG_031964.3:g.83532T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000310926.11:c.397+10T>C MANE Select ENSP00000311291.4:n.397+10T>C
ENST00000310926.8:c.397+10T>C ENSP00000311291.4:n.397+10T>C
ENST00000462770.5:n.520+10T>C
ENST00000464676.5:n.659+10T>C
ENST00000478651.1:n.520+10T>C
ENST00000481359.3:c.397+10T>C ENSP00000420028.3:n.397+10T>C
ENST00000493729.5:c.397+10T>C ENSP00000418893.1:n.397+10T>C
NM_005630.2:c.397+10T>C NP_005621.2:n.397+10T>C
XM_011513090.1:c.397+10T>C XP_011511392.1:n.397+10T>C
XM_017007077.1:c.-108+10T>C XP_016862566.1:n.-108+10T>C
XM_024453721.1:c.397+10T>C XP_024309489.1:n.397+10T>C
NM_005630.3:c.397+10T>C MANE Select NP_005621.2:n.397+10T>C