Canonical Allele Identifier: CA274819021

Gene: SLCO3A1

Linked Data

• dbSNP Id: rs933572429
• gnomAD v2: 15-92657473-T-A
• gnomAD v3: 15-92114243-T-A
• gnomAD v4: 15-92114243-T-A
• MyVariant Identifiers: chr15:g.92657473T>A (hg19) ; chr15:g.92114243T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92114243T>A , CM000677.2:g.92114243T>A	GRCh38
NC_000015.9:g.92657473T>A , CM000677.1:g.92657473T>A	GRCh37
NC_000015.8:g.90458477T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318445.11:c.1010-6222T>A MANE Select	ENSP00000320634.6:n.1010-6222T>A
ENST00000318445.10:c.1010-6222T>A	ENSP00000320634.6:n.1010-6222T>A
ENST00000424469.2:c.1010-6222T>A	ENSP00000387846.2:n.1010-6222T>A
ENST00000553653.5:n.1196-6222T>A
ENST00000555549.5:n.558-6222T>A
ENST00000555769.5:n.905-6222T>A
NM_001145044.1:c.1010-6222T>A	NP_001138516.1:n.1010-6222T>A
NM_013272.3:c.1010-6222T>A	NP_037404.2:n.1010-6222T>A
XM_005254889.1:c.1010-6222T>A	XP_005254946.1:n.1010-6222T>A
XM_005254891.1:c.665-6222T>A	XP_005254948.1:n.665-6222T>A
XM_011521456.1:c.836-6222T>A	XP_011519758.1:n.836-6222T>A
XM_011521457.1:c.1010-6222T>A	XP_011519759.1:n.1010-6222T>A
XR_429450.2:n.930-6222T>A
XR_931795.1:n.1100-6222T>A
XR_931796.1:n.1100-6222T>A
NR_135775.1:n.941-6222T>A
XM_005254891.3:c.665-6222T>A	XP_005254948.1:n.665-6222T>A
XM_011521456.2:c.836-6222T>A	XP_011519758.1:n.836-6222T>A
XR_931796.2:n.1100-6222T>A
NM_013272.4:c.1010-6222T>A MANE Select	NP_037404.2:n.1010-6222T>A
NR_135775.2:n.937-6222T>A