Canonical Allele Identifier: CA354620377
Community Standard Title: NM_005630.3(SLCO2A1):c.302T>G (p.Ile101Ser)
Gene: SLCO2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133973758A>C , CM000665.2:g.133973758A>C GRCh38
NC_000003.11:g.133692602A>C , CM000665.1:g.133692602A>C GRCh37
NC_000003.10:g.135175292A>C NCBI36
NG_031964.2:g.83427T>G
NG_031964.3:g.83427T>G

Transcript Alleles

HGVS Amino-acid Change
NM_005630.3:c.302T>G MANE Select NP_005621.2:p.Ile101Ser
ENST00000310926.11:c.302T>G MANE Select ENSP00000311291.4:p.Ile101Ser
NM_005630.2:c.302T>G NP_005621.2:p.Ile101Ser
ENST00000310926.8:c.302T>G ENSP00000311291.4:p.Ile101Ser
ENST00000462770.5:n.425T>G
ENST00000464676.5:n.564T>G
ENST00000478651.1:n.425T>G
ENST00000481359.3:c.302T>G ENSP00000420028.3:p.Ile101Ser
ENST00000493729.5:c.302T>G ENSP00000418893.1:p.Ile101Ser
XM_011513090.1:c.302T>G XP_011511392.1:p.Ile101Ser
XM_017007077.1:c.-203T>G XP_016862566.1:n.-203T>G
XM_024453721.1:c.302T>G XP_024309489.1:p.Ile101Ser