Canonical Allele Identifier: CA1245626109

Gene: CYP1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38071079C= , CM000664.2:g.38071079C=	GRCh38
NC_000002.11:g.38298222C= , CM000664.1:g.38298222C=	GRCh37
NC_000002.10:g.38151726C=	NCBI36
NG_008386.2:g.10023G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.1275G=	ENSP00000478839.2:p.Trp425=
ENST00000610745.5:c.1275G= MANE Select	ENSP00000478561.1:p.Trp425=
ENST00000492443.1:n.653G=
ENST00000494864.1:c.162G=	ENSP00000479876.1:p.Trp54=
ENST00000610745.4:c.1275G=	ENSP00000478561.1:p.Trp425=
ENST00000614273.1:c.1275G=	ENSP00000483678.1:p.Trp425=
NM_000104.3:c.1275G=	NP_000095.2:p.Trp425=
NM_000104.4:c.1275G= MANE Select	NP_000095.2:p.Trp425=