Canonical Allele Identifier: CA2586969157
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075269del , CM000664.2:g.38075269del GRCh38
NC_000002.11:g.38302412del , CM000664.1:g.38302412del GRCh37
NC_000002.10:g.38155916del NCBI36
NG_008386.2:g.5833del

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.120del ENSP00000478839.2:p.Arg41GlyfsTer19
ENST00000610745.5:c.120del MANE Select ENSP00000478561.1:p.Arg41GlyfsTer19
ENST00000490576.1:c.120del ENSP00000478839.1:p.Arg41GlyfsTer19
ENST00000494864.1:c.-70-3959del ENSP00000479876.1:n.-70-3959del
ENST00000610745.4:c.120del ENSP00000478561.1:p.Arg41GlyfsTer19
ENST00000613082.1:n.375+511del
ENST00000614273.1:c.120del ENSP00000483678.1:p.Arg41GlyfsTer19
NM_000104.3:c.120del NP_000095.2:p.Arg41GlyfsTer19
NM_000104.4:c.120del MANE Select NP_000095.2:p.Arg41GlyfsTer19