Canonical Allele Identifier: CA1789664463

Gene: CYP7B1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64616112T= , CM000670.2:g.64616112T=	GRCh38
NC_000008.10:g.65528669T= , CM000670.1:g.65528669T=	GRCh37
NC_000008.9:g.65691223T=	NCBI36
NG_008338.1:g.187680A=
NG_008338.2:g.187680A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310193.4:c.429A= MANE Select	ENSP00000310721.3:p.Gln143=
ENST00000310193.3:c.429A=	ENSP00000310721.3:p.Gln143=
NM_004820.3:c.429A=	NP_004811.1:p.Gln143=
NM_001324112.1:c.429A=	NP_001311041.1:p.Gln143=
NM_004820.4:c.429A=	NP_004811.1:p.Gln143=
XM_017014002.1:c.495A=	XP_016869491.1:p.Gln165=
NM_004820.5:c.429A= MANE Select	NP_004811.1:p.Gln143=
NM_001324112.2:c.429A=	NP_001311041.1:p.Gln143=