Canonical Allele Identifier: CA1245626150

Gene: CYP1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38071153G= , CM000664.2:g.38071153G=	GRCh38
NC_000002.11:g.38298296G= , CM000664.1:g.38298296G=	GRCh37
NC_000002.10:g.38151800G=	NCBI36
NG_008386.2:g.9949C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.1201C=	ENSP00000478839.2:p.His401=
ENST00000610745.5:c.1201C= MANE Select	ENSP00000478561.1:p.His401=
ENST00000492443.1:n.579C=
ENST00000494864.1:c.88C=	ENSP00000479876.1:p.His30=
ENST00000610745.4:c.1201C=	ENSP00000478561.1:p.His401=
ENST00000614273.1:c.1201C=	ENSP00000483678.1:p.His401=
NM_000104.3:c.1201C=	NP_000095.2:p.His401=
NM_000104.4:c.1201C= MANE Select	NP_000095.2:p.His401=