Canonical Allele Identifier: CA2626811
Community Standard Title: NM_005630.3(SLCO2A1):c.484C>G (p.Pro162Ala)
Gene: SLCO2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133955107G>C , CM000665.2:g.133955107G>C GRCh38
NC_000003.11:g.133673951G>C , CM000665.1:g.133673951G>C GRCh37
NC_000003.10:g.135156641G>C NCBI36
NG_031964.2:g.102078C>G
NG_031964.3:g.102078C>G

Transcript Alleles

HGVS Amino-acid Change
NM_005630.3:c.484C>G MANE Select NP_005621.2:p.Pro162Ala
ENST00000310926.11:c.484C>G MANE Select ENSP00000311291.4:p.Pro162Ala
NM_005630.2:c.484C>G NP_005621.2:p.Pro162Ala
ENST00000310926.8:c.484C>G ENSP00000311291.4:p.Pro162Ala
ENST00000462770.5:n.521-6407C>G
ENST00000464676.5:n.746C>G
ENST00000481359.3:c.484C>G ENSP00000420028.3:p.Pro162Ala
ENST00000493729.5:c.398-1346C>G ENSP00000418893.1:n.398-1346C>G
XM_011513090.1:c.484C>G XP_011511392.1:p.Pro162Ala
XM_017007077.1:c.-21C>G XP_016862566.1:n.-21C>G
XM_024453721.1:c.484C>G XP_024309489.1:p.Pro162Ala