Canonical Allele Identifier: CA1245626118

Gene: CYP1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38071091A= , CM000664.2:g.38071091A=	GRCh38
NC_000002.11:g.38298234A= , CM000664.1:g.38298234A=	GRCh37
NC_000002.10:g.38151738A=	NCBI36
NG_008386.2:g.10011T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.1263T=	ENSP00000478839.2:p.Phe421=
ENST00000610745.5:c.1263T= MANE Select	ENSP00000478561.1:p.Phe421=
ENST00000492443.1:n.641T=
ENST00000494864.1:c.150T=	ENSP00000479876.1:p.Phe50=
ENST00000610745.4:c.1263T=	ENSP00000478561.1:p.Phe421=
ENST00000614273.1:c.1263T=	ENSP00000483678.1:p.Phe421=
NM_000104.3:c.1263T=	NP_000095.2:p.Phe421=
NM_000104.4:c.1263T= MANE Select	NP_000095.2:p.Phe421=