Canonical Allele Identifier: CA1789664466

Gene: CYP7B1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64616130C= , CM000670.2:g.64616130C=	GRCh38
NC_000008.10:g.65528687C= , CM000670.1:g.65528687C=	GRCh37
NC_000008.9:g.65691241C=	NCBI36
NG_008338.1:g.187662G=
NG_008338.2:g.187662G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310193.4:c.411G= MANE Select	ENSP00000310721.3:p.Glu137=
ENST00000310193.3:c.411G=	ENSP00000310721.3:p.Glu137=
NM_004820.3:c.411G=	NP_004811.1:p.Glu137=
NM_001324112.1:c.411G=	NP_001311041.1:p.Glu137=
NM_004820.4:c.411G=	NP_004811.1:p.Glu137=
XM_017014002.1:c.477G=	XP_016869491.1:p.Glu159=
NM_004820.5:c.411G= MANE Select	NP_004811.1:p.Glu137=
NM_001324112.2:c.411G=	NP_001311041.1:p.Glu137=