Canonical Allele Identifier: CA15861430

Gene: SLCO3A1

Linked Data

• dbSNP Id: rs207954
• gnomAD v2: 15-92657373-T-C
• gnomAD v3: 15-92114143-T-C
• gnomAD v4: 15-92114143-T-C
• MyVariant Identifiers: chr15:g.92657373T>C (hg19) ; chr15:g.92114143T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92114143T>C , CM000677.2:g.92114143T>C	GRCh38
NC_000015.9:g.92657373T>C , CM000677.1:g.92657373T>C	GRCh37
NC_000015.8:g.90458377T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000318445.11:c.1010-6322T>C MANE Select	ENSP00000320634.6:n.1010-6322T>C
ENST00000318445.10:c.1010-6322T>C	ENSP00000320634.6:n.1010-6322T>C
ENST00000424469.2:c.1010-6322T>C	ENSP00000387846.2:n.1010-6322T>C
ENST00000553653.5:n.1196-6322T>C
ENST00000555549.5:n.558-6322T>C
ENST00000555769.5:n.905-6322T>C
NM_001145044.1:c.1010-6322T>C	NP_001138516.1:n.1010-6322T>C
NM_013272.3:c.1010-6322T>C	NP_037404.2:n.1010-6322T>C
XM_005254889.1:c.1010-6322T>C	XP_005254946.1:n.1010-6322T>C
XM_005254891.1:c.665-6322T>C	XP_005254948.1:n.665-6322T>C
XM_011521456.1:c.836-6322T>C	XP_011519758.1:n.836-6322T>C
XM_011521457.1:c.1010-6322T>C	XP_011519759.1:n.1010-6322T>C
XR_429450.2:n.930-6322T>C
XR_931795.1:n.1100-6322T>C
XR_931796.1:n.1100-6322T>C
NR_135775.1:n.941-6322T>C
XM_005254891.3:c.665-6322T>C	XP_005254948.1:n.665-6322T>C
XM_011521456.2:c.836-6322T>C	XP_011519758.1:n.836-6322T>C
XR_931796.2:n.1100-6322T>C
NM_013272.4:c.1010-6322T>C MANE Select	NP_037404.2:n.1010-6322T>C
NR_135775.2:n.937-6322T>C