Canonical Allele Identifier: CA1789668079

Gene: CYP7B1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64624595T= , CM000670.2:g.64624595T=	GRCh38
NC_000008.10:g.65537152T= , CM000670.1:g.65537152T=	GRCh37
NC_000008.9:g.65699706T=	NCBI36
NG_008338.1:g.179197A=
NG_008338.2:g.179197A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310193.4:c.123-56A= MANE Select	ENSP00000310721.3:n.123-56A=
ENST00000310193.3:c.123-56A=	ENSP00000310721.3:n.123-56A=
NM_004820.3:c.123-56A=	NP_004811.1:n.123-56A=
NM_001324112.1:c.123-56A=	NP_001311041.1:n.123-56A=
NM_004820.4:c.123-56A=	NP_004811.1:n.123-56A=
XM_017014002.1:c.189-56A=	XP_016869491.1:n.189-56A=
NM_004820.5:c.123-56A= MANE Select	NP_004811.1:n.123-56A=
NM_001324112.2:c.123-56A=	NP_001311041.1:n.123-56A=