Canonical Allele Identifier: CA6475288

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Linked Data

• dbSNP Id: rs768361956
• ExAC: 12:21015719 C / G
• gnomAD v2: 12-21015719-C-G
• MyVariant Identifiers: chr12:g.21015719C>G (hg19) ; chr12:g.20862785C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20862785C>G , CM000674.2:g.20862785C>G	GRCh38
NC_000012.11:g.21015719C>G , CM000674.1:g.21015719C>G	GRCh37
NC_000012.10:g.20906986C>G	NCBI36
NG_032071.1:g.57082C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381545.8:c.658C>G (SLCO1B3) MANE Select	ENSP00000370956.4:p.Pro220Ala
ENST00000261196.6:c.658C>G (SLCO1B3)	ENSP00000261196.2:p.Pro220Ala
ENST00000381541.7:c.359+4214C>G (SLCO1B3-SLCO1B7)	ENSP00000370952.3:n.359+4214C>G
ENST00000381545.7:c.658C>G (SLCO1B3)	ENSP00000370956.3:p.Pro220Ala
ENST00000540229.1:c.658C>G (SLCO1B3-SLCO1B7)	ENSP00000441269.1:p.Pro220Ala
ENST00000540853.5:c.658C>G (SLCO1B3)	ENSP00000442000.1:p.Pro220Ala
ENST00000544370.1:c.130C>G (SLCO1B3)	ENSP00000443225.1:p.Pro44Ala
NM_019844.3:c.658C>G (SLCO1B3)	NP_062818.1:p.Pro220Ala
NM_001349920.1:c.574C>G (SLCO1B3)	NP_001336849.1:p.Pro192Ala
NM_001349920.2:c.574C>G (SLCO1B3)	NP_001336849.1:p.Pro192Ala
NM_001371097.1:c.658C>G (SLCO1B3-SLCO1B7)	NP_001358026.1:p.Pro220Ala
NM_019844.4:c.658C>G (SLCO1B3) MANE Select	NP_062818.1:p.Pro220Ala