Canonical Allele Identifier: CA1789668028

Gene: CYP7B1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64624486A= , CM000670.2:g.64624486A=	GRCh38
NC_000008.10:g.65537043A= , CM000670.1:g.65537043A=	GRCh37
NC_000008.9:g.65699597A=	NCBI36
NG_008338.1:g.179306T=
NG_008338.2:g.179306T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310193.4:c.176T= MANE Select	ENSP00000310721.3:p.Val59=
ENST00000310193.3:c.176T=	ENSP00000310721.3:p.Val59=
NM_004820.3:c.176T=	NP_004811.1:p.Val59=
NM_001324112.1:c.176T=	NP_001311041.1:p.Val59=
NM_004820.4:c.176T=	NP_004811.1:p.Val59=
XM_017014002.1:c.242T=	XP_016869491.1:p.Val81=
NM_004820.5:c.176T= MANE Select	NP_004811.1:p.Val59=
NM_001324112.2:c.176T=	NP_001311041.1:p.Val59=