Canonical Allele Identifier: CA1245628157
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075082T= , CM000664.2:g.38075082T= GRCh38
NC_000002.11:g.38302225T= , CM000664.1:g.38302225T= GRCh37
NC_000002.10:g.38155729T= NCBI36
NG_008386.2:g.6020A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.307A= ENSP00000478839.2:p.Ile103=
ENST00000610745.5:c.307A= MANE Select ENSP00000478561.1:p.Ile103=
ENST00000490576.1:c.307A= ENSP00000478839.1:p.Ile103=
ENST00000494864.1:c.-70-3772A= ENSP00000479876.1:n.-70-3772A=
ENST00000610745.4:c.307A= ENSP00000478561.1:p.Ile103=
ENST00000613082.1:n.376-674A=
ENST00000614273.1:c.307A= ENSP00000483678.1:p.Ile103=
NM_000104.3:c.307A= NP_000095.2:p.Ile103=
NM_000104.4:c.307A= MANE Select NP_000095.2:p.Ile103=