Canonical Allele Identifier: CA224629693

Gene: SLCO2B1

Linked Data

• dbSNP Id: rs539510429
• gnomAD v2: 11-74907489-C-T
• gnomAD v3: 11-75196444-C-T
• gnomAD v4: 11-75196444-C-T
• MyVariant Identifiers: chr11:g.74907489C>T (hg19) ; chr11:g.75196444C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75196444C>T , CM000673.2:g.75196444C>T	GRCh38
NC_000011.9:g.74907489C>T , CM000673.1:g.74907489C>T	GRCh37
NC_000011.8:g.74585137C>T	NCBI36
NG_027921.1:g.50458C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1434-70C>T MANE Select	ENSP00000289575.5:n.1434-70C>T
ENST00000289575.9:c.1434-70C>T	ENSP00000289575.5:n.1434-70C>T
ENST00000428359.6:c.1368-70C>T	ENSP00000388912.2:n.1368-70C>T
ENST00000454962.6:c.753-70C>T	ENSP00000389653.2:n.753-70C>T
ENST00000525650.5:c.1002-70C>T	ENSP00000436324.1:n.1002-70C>T
ENST00000528108.1:n.170C>T
ENST00000530012.1:n.191C>T
ENST00000531756.5:n.981-70C>T
ENST00000532236.5:c.1086-70C>T	ENSP00000434112.1:n.1086-70C>T
NM_001145211.2:c.1368-70C>T	NP_001138683.1:n.1368-70C>T
NM_001145212.2:c.1002-70C>T	NP_001138684.1:n.1002-70C>T
NM_007256.4:c.1434-70C>T	NP_009187.1:n.1434-70C>T
XM_017017157.1:c.1440-70C>T	XP_016872646.1:n.1440-70C>T
NM_001145211.3:c.1368-70C>T	NP_001138683.1:n.1368-70C>T
NM_001145212.3:c.1002-70C>T	NP_001138684.1:n.1002-70C>T
NM_007256.5:c.1434-70C>T MANE Select	NP_009187.1:n.1434-70C>T