Canonical Allele Identifier: CA1245628178
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075109T= , CM000664.2:g.38075109T= GRCh38
NC_000002.11:g.38302252T= , CM000664.1:g.38302252T= GRCh37
NC_000002.10:g.38155756T= NCBI36
NG_008386.2:g.5993A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.280A= ENSP00000478839.2:p.Ile94=
ENST00000610745.5:c.280A= MANE Select ENSP00000478561.1:p.Ile94=
ENST00000490576.1:c.280A= ENSP00000478839.1:p.Ile94=
ENST00000494864.1:c.-70-3799A= ENSP00000479876.1:n.-70-3799A=
ENST00000610745.4:c.280A= ENSP00000478561.1:p.Ile94=
ENST00000613082.1:n.375+671A=
ENST00000614273.1:c.280A= ENSP00000483678.1:p.Ile94=
NM_000104.3:c.280A= NP_000095.2:p.Ile94=
NM_000104.4:c.280A= MANE Select NP_000095.2:p.Ile94=