Canonical Allele Identifier: CA2626634
Community Standard Title: NM_005630.3(SLCO2A1):c.904G>C (p.Ala302Pro)
Gene: SLCO2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133948929C>G , CM000665.2:g.133948929C>G GRCh38
NC_000003.11:g.133667773C>G , CM000665.1:g.133667773C>G GRCh37
NC_000003.10:g.135150463C>G NCBI36
NG_031964.2:g.108256G>C
NG_031964.3:g.108256G>C

Transcript Alleles

HGVS Amino-acid Change
NM_005630.3:c.904G>C MANE Select NP_005621.2:p.Ala302Pro
ENST00000310926.11:c.904G>C MANE Select ENSP00000311291.4:p.Ala302Pro
NM_005630.2:c.904G>C NP_005621.2:p.Ala302Pro
ENST00000310926.8:c.904G>C ENSP00000311291.4:p.Ala302Pro
ENST00000462770.5:n.521-229G>C
ENST00000477061.1:n.288G>C
ENST00000481359.3:c.904G>C ENSP00000420028.3:p.Ala302Pro
ENST00000493729.5:c.676G>C ENSP00000418893.1:p.Ala226Pro
XM_011513090.1:c.904G>C XP_011511392.1:p.Ala302Pro
XM_017007077.1:c.400G>C XP_016862566.1:p.Ala134Pro
XM_024453721.1:c.904G>C XP_024309489.1:p.Ala302Pro