Canonical Allele Identifier: CA1245626049

Gene: CYP1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38070973T= , CM000664.2:g.38070973T=	GRCh38
NC_000002.11:g.38298116T= , CM000664.1:g.38298116T=	GRCh37
NC_000002.10:g.38151620T=	NCBI36
NG_008386.2:g.10129A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.1381A=	ENSP00000478839.2:p.Met461=
ENST00000610745.5:c.1381A= MANE Select	ENSP00000478561.1:p.Met461=
ENST00000494864.1:c.268A=	ENSP00000479876.1:p.Met90=
ENST00000610745.4:c.1381A=	ENSP00000478561.1:p.Met461=
ENST00000614273.1:c.1381A=	ENSP00000483678.1:p.Met461=
NM_000104.3:c.1381A=	NP_000095.2:p.Met461=
NM_000104.4:c.1381A= MANE Select	NP_000095.2:p.Met461=