Canonical Allele Identifier: CA2617888049

Gene: SLCO1B3 SLCO1B3-SLCO1B7

Linked Data

• gnomAD v4: 12-20858635-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.20858640del , CM000674.2:g.20858640del	GRCh38
NC_000012.11:g.21011574del , CM000674.1:g.21011574del	GRCh37
NC_000012.10:g.20902841del	NCBI36
NG_032071.1:g.52937del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381545.8:c.359+69del (SLCO1B3) MANE Select	ENSP00000370956.4:n.359+69del
ENST00000261196.6:c.359+69del (SLCO1B3)	ENSP00000261196.2:n.359+69del
ENST00000381541.7:c.359+69del (SLCO1B3-SLCO1B7)	ENSP00000370952.3:n.359+69del
ENST00000381545.7:c.359+69del (SLCO1B3)	ENSP00000370956.3:n.359+69del
ENST00000540229.1:c.359+69del (SLCO1B3-SLCO1B7)	ENSP00000441269.1:n.359+69del
ENST00000540853.5:c.359+69del (SLCO1B3)	ENSP00000442000.1:n.359+69del
ENST00000545880.1:n.211+69del (SLCO1B3)
NM_019844.3:c.359+69del (SLCO1B3)	NP_062818.1:n.359+69del
NM_001349920.1:c.275+69del (SLCO1B3)	NP_001336849.1:n.275+69del
NM_001349920.2:c.275+69del (SLCO1B3)	NP_001336849.1:n.275+69del
NM_001371097.1:c.359+69del (SLCO1B3-SLCO1B7)	NP_001358026.1:n.359+69del
NM_019844.4:c.359+69del (SLCO1B3) MANE Select	NP_062818.1:n.359+69del