Canonical Allele Identifier: CA1789659736

Gene: CYP7B1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64604829C= , CM000670.2:g.64604829C=	GRCh38
NC_000008.10:g.65517386C= , CM000670.1:g.65517386C=	GRCh37
NC_000008.9:g.65679940C=	NCBI36
NG_008338.1:g.198963G=
NG_008338.2:g.198963G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000310193.4:c.1086G= MANE Select	ENSP00000310721.3:p.Leu362=
ENST00000310193.3:c.1086G=	ENSP00000310721.3:p.Leu362=
ENST00000523954.1:n.360G=
NM_004820.3:c.1086G=	NP_004811.1:p.Leu362=
NM_001324112.1:c.1086G=	NP_001311041.1:p.Leu362=
NM_004820.4:c.1086G=	NP_004811.1:p.Leu362=
XM_017014002.1:c.1152G=	XP_016869491.1:p.Leu384=
NM_004820.5:c.1086G= MANE Select	NP_004811.1:p.Leu362=
NM_001324112.2:c.1086G=	NP_001311041.1:p.Leu362=