Canonical Allele Identifier: CA381871144

Gene: SLCO2B1

Linked Data

• MyVariant Identifiers: chr11:g.74907593A>T (hg19) ; chr11:g.75196548A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75196548A>T , CM000673.2:g.75196548A>T	GRCh38
NC_000011.9:g.74907593A>T , CM000673.1:g.74907593A>T	GRCh37
NC_000011.8:g.74585241A>T	NCBI36
NG_027921.1:g.50562A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000289575.10:c.1468A>T MANE Select	ENSP00000289575.5:p.Met490Leu
ENST00000289575.9:c.1468A>T	ENSP00000289575.5:p.Met490Leu
ENST00000428359.6:c.1402A>T	ENSP00000388912.2:p.Met468Leu
ENST00000454962.6:c.787A>T	ENSP00000389653.2:p.Met263Leu
ENST00000525650.5:c.1036A>T	ENSP00000436324.1:p.Met346Leu
ENST00000528108.1:n.274A>T
ENST00000530012.1:n.295A>T
ENST00000531756.5:n.1015A>T
ENST00000532236.5:c.1120A>T	ENSP00000434112.1:p.Met374Leu
NM_001145211.2:c.1402A>T	NP_001138683.1:p.Met468Leu
NM_001145212.2:c.1036A>T	NP_001138684.1:p.Met346Leu
NM_007256.4:c.1468A>T	NP_009187.1:p.Met490Leu
XM_017017157.1:c.1474A>T	XP_016872646.1:p.Met492Leu
NM_001145211.3:c.1402A>T	NP_001138683.1:p.Met468Leu
NM_001145212.3:c.1036A>T	NP_001138684.1:p.Met346Leu
NM_007256.5:c.1468A>T MANE Select	NP_009187.1:p.Met490Leu