Canonical Allele Identifier: CA354617930
Gene: SLCO2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133953723C>G , CM000665.2:g.133953723C>G GRCh38
NC_000003.11:g.133672567C>G , CM000665.1:g.133672567C>G GRCh37
NC_000003.10:g.135155257C>G NCBI36
NG_031964.2:g.103462G>C
NG_031964.3:g.103462G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000310926.11:c.664G>C MANE Select ENSP00000311291.4:p.Gly222Arg
ENST00000310926.8:c.664G>C ENSP00000311291.4:p.Gly222Arg
ENST00000462770.5:n.521-5023G>C
ENST00000464676.5:n.926G>C
ENST00000481359.3:c.664G>C ENSP00000420028.3:p.Gly222Arg
ENST00000493729.5:c.436G>C ENSP00000418893.1:p.Gly146Arg
NM_005630.2:c.664G>C NP_005621.2:p.Gly222Arg
XM_011513090.1:c.664G>C XP_011511392.1:p.Gly222Arg
XM_017007077.1:c.160G>C XP_016862566.1:p.Gly54Arg
XM_024453721.1:c.664G>C XP_024309489.1:p.Gly222Arg
NM_005630.3:c.664G>C MANE Select NP_005621.2:p.Gly222Arg