Canonical Allele Identifier: CA1245628146
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075064G= , CM000664.2:g.38075064G= GRCh38
NC_000002.11:g.38302207G= , CM000664.1:g.38302207G= GRCh37
NC_000002.10:g.38155711G= NCBI36
NG_008386.2:g.6038C=

Transcript Alleles

HGVS Amino-acid change
ENST00000490576.2:c.325C= ENSP00000478839.2:p.Gln109=
ENST00000610745.5:c.325C= MANE Select ENSP00000478561.1:p.Gln109=
ENST00000490576.1:c.325C= ENSP00000478839.1:p.Gln109=
ENST00000494864.1:c.-70-3754C= ENSP00000479876.1:n.-70-3754C=
ENST00000610745.4:c.325C= ENSP00000478561.1:p.Gln109=
ENST00000613082.1:n.376-656C=
ENST00000614273.1:c.325C= ENSP00000483678.1:p.Gln109=
NM_000104.3:c.325C= NP_000095.2:p.Gln109=
NM_000104.4:c.325C= MANE Select NP_000095.2:p.Gln109=