Canonical Allele Identifier: CA1789668001

Gene: CYP7B1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64624423G= , CM000670.2:g.64624423G=	GRCh38
NC_000008.10:g.65536980G= , CM000670.1:g.65536980G=	GRCh37
NC_000008.9:g.65699534G=	NCBI36
NG_008338.1:g.179369C=
NG_008338.2:g.179369C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310193.4:c.239C= MANE Select	ENSP00000310721.3:p.Thr80=
ENST00000310193.3:c.239C=	ENSP00000310721.3:p.Thr80=
NM_004820.3:c.239C=	NP_004811.1:p.Thr80=
NM_001324112.1:c.239C=	NP_001311041.1:p.Thr80=
NM_004820.4:c.239C=	NP_004811.1:p.Thr80=
XM_017014002.1:c.305C=	XP_016869491.1:p.Thr102=
NM_004820.5:c.239C= MANE Select	NP_004811.1:p.Thr80=
NM_001324112.2:c.239C=	NP_001311041.1:p.Thr80=