Canonical Allele Identifier: CA1245626230
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38071306G= , CM000664.2:g.38071306G= GRCh38
NC_000002.11:g.38298449G= , CM000664.1:g.38298449G= GRCh37
NC_000002.10:g.38151953G= NCBI36
NG_008386.2:g.9796C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.1048C= ENSP00000478839.2:p.Pro350=
ENST00000610745.5:c.1048C= MANE Select ENSP00000478561.1:p.Pro350=
ENST00000492443.1:n.426C=
ENST00000494864.1:c.-66C= ENSP00000479876.1:n.-66C=
ENST00000610745.4:c.1048C= ENSP00000478561.1:p.Pro350=
ENST00000613082.1:n.443C=
ENST00000614273.1:c.1048C= ENSP00000483678.1:p.Pro350=
NM_000104.3:c.1048C= NP_000095.2:p.Pro350=
NM_000104.4:c.1048C= MANE Select NP_000095.2:p.Pro350=