Canonical Allele Identifier: CA2615134161

Gene: SLCO2B1

Linked Data

• gnomAD v4: 11-75196441-GGCCGAGGAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75196445_75196453del , CM000673.2:g.75196445_75196453del	GRCh38
NC_000011.9:g.74907490_74907498del , CM000673.1:g.74907490_74907498del	GRCh37
NC_000011.8:g.74585138_74585146del	NCBI36
NG_027921.1:g.50459_50467del

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1434-69_1434-61del MANE Select	ENSP00000289575.5:n.1434-69_1434-61del
ENST00000289575.9:c.1434-69_1434-61del	ENSP00000289575.5:n.1434-69_1434-61del
ENST00000428359.6:c.1368-69_1368-61del	ENSP00000388912.2:n.1368-69_1368-61del
ENST00000454962.6:c.753-69_753-61del	ENSP00000389653.2:n.753-69_753-61del
ENST00000525650.5:c.1002-69_1002-61del	ENSP00000436324.1:n.1002-69_1002-61del
ENST00000528108.1:n.171_179del
ENST00000530012.1:n.192_200del
ENST00000531756.5:n.981-69_981-61del
ENST00000532236.5:c.1086-69_1086-61del	ENSP00000434112.1:n.1086-69_1086-61del
NM_001145211.2:c.1368-69_1368-61del	NP_001138683.1:n.1368-69_1368-61del
NM_001145212.2:c.1002-69_1002-61del	NP_001138684.1:n.1002-69_1002-61del
NM_007256.4:c.1434-69_1434-61del	NP_009187.1:n.1434-69_1434-61del
XM_017017157.1:c.1440-69_1440-61del	XP_016872646.1:n.1440-69_1440-61del
NM_001145211.3:c.1368-69_1368-61del	NP_001138683.1:n.1368-69_1368-61del
NM_001145212.3:c.1002-69_1002-61del	NP_001138684.1:n.1002-69_1002-61del
NM_007256.5:c.1434-69_1434-61del MANE Select	NP_009187.1:n.1434-69_1434-61del