Canonical Allele Identifier: CA686395458

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Linked Data

• dbSNP Id: rs1438606221
• gnomAD v3: 12-20863361-CAAAT-C
• gnomAD v4: 12-20863361-CAAAT-C
• MyVariant Identifiers: chr12:g.21016296_21016299del (hg19) ; chr12:g.20863362_20863365del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20863362_20863365del , CM000674.2:g.20863362_20863365del	GRCh38
NC_000012.11:g.21016296_21016299del , CM000674.1:g.21016296_21016299del	GRCh37
NC_000012.10:g.20907563_20907566del	NCBI36
NG_032071.1:g.57659_57662del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381545.8:c.727+508_727+511del (SLCO1B3) MANE Select	ENSP00000370956.4:n.727+508_727+511del
ENST00000261196.6:c.727+508_727+511del (SLCO1B3)	ENSP00000261196.2:n.727+508_727+511del
ENST00000381541.7:c.359+4791_359+4794del (SLCO1B3-SLCO1B7)	ENSP00000370952.3:n.359+4791_359+4794del
ENST00000381545.7:c.727+508_727+511del (SLCO1B3)	ENSP00000370956.3:n.727+508_727+511del
ENST00000540229.1:c.727+508_727+511del (SLCO1B3-SLCO1B7)	ENSP00000441269.1:n.727+508_727+511del
ENST00000540853.5:c.727+508_727+511del (SLCO1B3)	ENSP00000442000.1:n.727+508_727+511del
ENST00000544370.1:c.199+508_199+511del (SLCO1B3)	ENSP00000443225.1:n.199+508_199+511del
NM_019844.3:c.727+508_727+511del (SLCO1B3)	NP_062818.1:n.727+508_727+511del
NM_001349920.1:c.643+508_643+511del (SLCO1B3)	NP_001336849.1:n.643+508_643+511del
NM_001349920.2:c.643+508_643+511del (SLCO1B3)	NP_001336849.1:n.643+508_643+511del
NM_001371097.1:c.727+508_727+511del (SLCO1B3-SLCO1B7)	NP_001358026.1:n.727+508_727+511del
NM_019844.4:c.727+508_727+511del (SLCO1B3) MANE Select	NP_062818.1:n.727+508_727+511del