Canonical Allele Identifier: CA2586969155
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075238dup , CM000664.2:g.38075238dup GRCh38
NC_000002.11:g.38302381dup , CM000664.1:g.38302381dup GRCh37
NC_000002.10:g.38155885dup NCBI36
NG_008386.2:g.5868dup

Transcript Alleles

HGVS Amino-acid change
ENST00000490576.2:c.155dup ENSP00000478839.2:p.Phe55ValfsTer?
ENST00000610745.5:c.155dup MANE Select ENSP00000478561.1:p.Phe55ValfsTer?
ENST00000490576.1:c.155dup ENSP00000478839.1:p.Phe55ValfsTer?
ENST00000494864.1:c.-70-3924dup ENSP00000479876.1:n.-70-3924dup
ENST00000610745.4:c.155dup ENSP00000478561.1:p.Phe55ValfsTer?
ENST00000613082.1:n.375+546dup
ENST00000614273.1:c.155dup ENSP00000483678.1:p.Phe55ValfsTer?
NM_000104.3:c.155dup NP_000095.2:p.Phe55ValfsTer?
NM_000104.4:c.155dup MANE Select NP_000095.2:p.Phe55ValfsTer?