Canonical Allele Identifier: CA1245628040
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38074889T= , CM000664.2:g.38074889T= GRCh38
NC_000002.11:g.38302032T= , CM000664.1:g.38302032T= GRCh37
NC_000002.10:g.38155536T= NCBI36
NG_008386.2:g.6213A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.500A= ENSP00000478839.2:p.Glu167=
ENST00000610745.5:c.500A= MANE Select ENSP00000478561.1:p.Glu167=
ENST00000494864.1:c.-70-3579A= ENSP00000479876.1:n.-70-3579A=
ENST00000610745.4:c.500A= ENSP00000478561.1:p.Glu167=
ENST00000613082.1:n.376-481A=
ENST00000614273.1:c.500A= ENSP00000483678.1:p.Glu167=
NM_000104.3:c.500A= NP_000095.2:p.Glu167=
NM_000104.4:c.500A= MANE Select NP_000095.2:p.Glu167=