Canonical Allele Identifier: CA1245626064
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38071006C= , CM000664.2:g.38071006C= GRCh38
NC_000002.11:g.38298149C= , CM000664.1:g.38298149C= GRCh37
NC_000002.10:g.38151653C= NCBI36
NG_008386.2:g.10096G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.1348G= ENSP00000478839.2:p.Gly450=
ENST00000610745.5:c.1348G= MANE Select ENSP00000478561.1:p.Gly450=
ENST00000492443.1:n.726G=
ENST00000494864.1:c.235G= ENSP00000479876.1:p.Gly79=
ENST00000610745.4:c.1348G= ENSP00000478561.1:p.Gly450=
ENST00000614273.1:c.1348G= ENSP00000483678.1:p.Gly450=
NM_000104.3:c.1348G= NP_000095.2:p.Gly450=
NM_000104.4:c.1348G= MANE Select NP_000095.2:p.Gly450=