Canonical Allele Identifier: CA1789664425

Gene: CYP7B1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64616029T= , CM000670.2:g.64616029T=	GRCh38
NC_000008.10:g.65528586T= , CM000670.1:g.65528586T=	GRCh37
NC_000008.9:g.65691140T=	NCBI36
NG_008338.1:g.187763A=
NG_008338.2:g.187763A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310193.4:c.512A= MANE Select	ENSP00000310721.3:p.Lys171=
ENST00000310193.3:c.512A=	ENSP00000310721.3:p.Lys171=
NM_004820.3:c.512A=	NP_004811.1:p.Lys171=
NM_001324112.1:c.512A=	NP_001311041.1:p.Lys171=
NM_004820.4:c.512A=	NP_004811.1:p.Lys171=
XM_017014002.1:c.578A=	XP_016869491.1:p.Lys193=
NM_004820.5:c.512A= MANE Select	NP_004811.1:p.Lys171=
NM_001324112.2:c.512A=	NP_001311041.1:p.Lys171=