Canonical Allele Identifier: CA354615539
Community Standard Title: NM_005630.3(SLCO2A1):c.1668G>C (p.Gln556His)
Gene: SLCO2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133938451C>G , CM000665.2:g.133938451C>G GRCh38
NC_000003.11:g.133657295C>G , CM000665.1:g.133657295C>G GRCh37
NC_000003.10:g.135139985C>G NCBI36
NG_031964.2:g.118734G>C
NG_031964.3:g.118734G>C

Transcript Alleles

HGVS Amino-acid Change
NM_005630.3:c.1668G>C MANE Select NP_005621.2:p.Gln556His
ENST00000310926.11:c.1668G>C MANE Select ENSP00000311291.4:p.Gln556His
NM_005630.2:c.1668G>C NP_005621.2:p.Gln556His
ENST00000310926.8:c.1668G>C ENSP00000311291.4:p.Gln556His
ENST00000481359.3:c.*230G>C ENSP00000420028.3:n.*230G>C
ENST00000493729.5:c.1440G>C ENSP00000418893.1:p.Gln480His
XM_011513090.1:c.1668G>C XP_011511392.1:p.Gln556His
XM_017007077.1:c.1164G>C XP_016862566.1:p.Gln388His
XM_024453721.1:c.1668G>C XP_024309489.1:p.Gln556His