Canonical Allele Identifier: CA1789668003

Gene: CYP7B1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64624426T= , CM000670.2:g.64624426T=	GRCh38
NC_000008.10:g.65536983T= , CM000670.1:g.65536983T=	GRCh37
NC_000008.9:g.65699537T=	NCBI36
NG_008338.1:g.179366A=
NG_008338.2:g.179366A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310193.4:c.236A= MANE Select	ENSP00000310721.3:p.Asp79=
ENST00000310193.3:c.236A=	ENSP00000310721.3:p.Asp79=
NM_004820.3:c.236A=	NP_004811.1:p.Asp79=
NM_001324112.1:c.236A=	NP_001311041.1:p.Asp79=
NM_004820.4:c.236A=	NP_004811.1:p.Asp79=
XM_017014002.1:c.302A=	XP_016869491.1:p.Asp101=
NM_004820.5:c.236A= MANE Select	NP_004811.1:p.Asp79=
NM_001324112.2:c.236A=	NP_001311041.1:p.Asp79=