Canonical Allele Identifier: CA1245628252

Gene: CYP1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38075218C= , CM000664.2:g.38075218C=	GRCh38
NC_000002.11:g.38302361C= , CM000664.1:g.38302361C=	GRCh37
NC_000002.10:g.38155865C=	NCBI36
NG_008386.2:g.5884G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.171G=	ENSP00000478839.2:p.Trp57=
ENST00000610745.5:c.171G= MANE Select	ENSP00000478561.1:p.Trp57=
ENST00000490576.1:c.171G=	ENSP00000478839.1:p.Trp57=
ENST00000494864.1:c.-70-3908G=	ENSP00000479876.1:n.-70-3908G=
ENST00000610745.4:c.171G=	ENSP00000478561.1:p.Trp57=
ENST00000613082.1:n.375+562G=
ENST00000614273.1:c.171G=	ENSP00000483678.1:p.Trp57=
NM_000104.3:c.171G=	NP_000095.2:p.Trp57=
NM_000104.4:c.171G= MANE Select	NP_000095.2:p.Trp57=