Canonical Allele Identifier: CA346327712
Gene: CYP1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38071183A>T , CM000664.2:g.38071183A>T GRCh38
NC_000002.11:g.38298326A>T , CM000664.1:g.38298326A>T GRCh37
NC_000002.10:g.38151830A>T NCBI36
NG_008386.2:g.9919T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.1171T>A ENSP00000478839.2:p.Phe391Ile
ENST00000610745.5:c.1171T>A MANE Select ENSP00000478561.1:p.Phe391Ile
ENST00000492443.1:n.549T>A
ENST00000494864.1:c.58T>A ENSP00000479876.1:p.Phe20Ile
ENST00000610745.4:c.1171T>A ENSP00000478561.1:p.Phe391Ile
ENST00000613082.1:n.566T>A
ENST00000614273.1:c.1171T>A ENSP00000483678.1:p.Phe391Ile
NM_000104.3:c.1171T>A NP_000095.2:p.Phe391Ile
NM_000104.4:c.1171T>A MANE Select NP_000095.2:p.Phe391Ile