Canonical Allele Identifier: CA1789667991

Gene: CYP7B1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64624401A= , CM000670.2:g.64624401A=	GRCh38
NC_000008.10:g.65536958A= , CM000670.1:g.65536958A=	GRCh37
NC_000008.9:g.65699512A=	NCBI36
NG_008338.1:g.179391T=
NG_008338.2:g.179391T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310193.4:c.259+2T= MANE Select	ENSP00000310721.3:n.259+2T=
ENST00000310193.3:c.259+2T=	ENSP00000310721.3:n.259+2T=
NM_004820.3:c.259+2T=	NP_004811.1:n.259+2T=
NM_001324112.1:c.259+2T=	NP_001311041.1:n.259+2T=
NM_004820.4:c.259+2T=	NP_004811.1:n.259+2T=
XM_017014002.1:c.325+2T=	XP_016869491.1:n.325+2T=
NM_004820.5:c.259+2T= MANE Select	NP_004811.1:n.259+2T=
NM_001324112.2:c.259+2T=	NP_001311041.1:n.259+2T=