Canonical Allele Identifier: CA1245628102

Gene: CYP1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38075000C= , CM000664.2:g.38075000C=	GRCh38
NC_000002.11:g.38302143C= , CM000664.1:g.38302143C=	GRCh37
NC_000002.10:g.38155647C=	NCBI36
NG_008386.2:g.6102G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.389G=	ENSP00000478839.2:p.Arg130=
ENST00000610745.5:c.389G= MANE Select	ENSP00000478561.1:p.Arg130=
ENST00000490576.1:c.389G=	ENSP00000478839.1:p.Arg130=
ENST00000494864.1:c.-70-3690G=	ENSP00000479876.1:n.-70-3690G=
ENST00000610745.4:c.389G=	ENSP00000478561.1:p.Arg130=
ENST00000613082.1:n.376-592G=
ENST00000614273.1:c.389G=	ENSP00000483678.1:p.Arg130=
NM_000104.3:c.389G=	NP_000095.2:p.Arg130=
NM_000104.4:c.389G= MANE Select	NP_000095.2:p.Arg130=