Canonical Allele Identifier: CA11603371
Community Standard Title: NM_005630.3(SLCO2A1):c.1626-295A>G
Gene: SLCO2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133938788T>C , CM000665.2:g.133938788T>C GRCh38
NC_000003.11:g.133657632T>C , CM000665.1:g.133657632T>C GRCh37
NC_000003.10:g.135140322T>C NCBI36
NG_031964.2:g.118397A>G
NG_031964.3:g.118397A>G

Transcript Alleles

HGVS Amino-acid Change
NM_005630.3:c.1626-295A>G MANE Select NP_005621.2:n.1626-295A>G
ENST00000310926.11:c.1626-295A>G MANE Select ENSP00000311291.4:n.1626-295A>G
NM_005630.2:c.1626-295A>G NP_005621.2:n.1626-295A>G
ENST00000310926.8:c.1626-295A>G ENSP00000311291.4:n.1626-295A>G
ENST00000481359.3:c.*188-295A>G ENSP00000420028.3:n.*188-295A>G
ENST00000493729.5:c.1398-295A>G ENSP00000418893.1:n.1398-295A>G
XM_011513090.1:c.1626-295A>G XP_011511392.1:n.1626-295A>G
XM_017007077.1:c.1122-295A>G XP_016862566.1:n.1122-295A>G
XM_024453721.1:c.1626-295A>G XP_024309489.1:n.1626-295A>G