Canonical Allele Identifier: CA1245625989
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38070865G= , CM000664.2:g.38070865G= GRCh38
NC_000002.11:g.38298008G= , CM000664.1:g.38298008G= GRCh37
NC_000002.10:g.38151512G= NCBI36
NG_008386.2:g.10237C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.1489C= ENSP00000478839.2:p.Pro497=
ENST00000610745.5:c.1489C= MANE Select ENSP00000478561.1:p.Pro497=
ENST00000494864.1:c.376C= ENSP00000479876.1:p.Pro126=
ENST00000610745.4:c.1489C= ENSP00000478561.1:p.Pro497=
ENST00000614273.1:c.1489C= ENSP00000483678.1:p.Pro497=
NM_000104.3:c.1489C= NP_000095.2:p.Pro497=
NM_000104.4:c.1489C= MANE Select NP_000095.2:p.Pro497=