Canonical Allele Identifier: CA354615993
Community Standard Title: NM_005630.3(SLCO2A1):c.1461+1G>C
Gene: SLCO2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133945094C>G , CM000665.2:g.133945094C>G GRCh38
NC_000003.11:g.133663938C>G , CM000665.1:g.133663938C>G GRCh37
NC_000003.10:g.135146628C>G NCBI36
NG_031964.2:g.112091G>C
NG_031964.3:g.112091G>C

Transcript Alleles

HGVS Amino-acid Change
NM_005630.3:c.1461+1G>C MANE Select NP_005621.2:n.1461+1G>C
ENST00000310926.11:c.1461+1G>C MANE Select ENSP00000311291.4:n.1461+1G>C
NM_005630.2:c.1461+1G>C NP_005621.2:n.1461+1G>C
ENST00000310926.8:c.1461+1G>C ENSP00000311291.4:n.1461+1G>C
ENST00000462770.5:n.1041+1G>C
ENST00000481359.3:c.*23+1G>C ENSP00000420028.3:n.*23+1G>C
ENST00000493729.5:c.1233+1G>C ENSP00000418893.1:n.1233+1G>C
XM_011513090.1:c.1461+1G>C XP_011511392.1:n.1461+1G>C
XM_017007077.1:c.957+1G>C XP_016862566.1:n.957+1G>C
XM_024453721.1:c.1461+1G>C XP_024309489.1:n.1461+1G>C