Canonical Allele Identifier: CA3006920441
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075157_38075158del , CM000664.2:g.38075157_38075158del GRCh38
NC_000002.11:g.38302300_38302301del , CM000664.1:g.38302300_38302301del GRCh37
NC_000002.10:g.38155804_38155805del NCBI36
NG_008386.2:g.5944_5945del

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.231_232del ENSP00000478839.2:p.Arg79AlafsTer?
ENST00000610745.5:c.231_232del MANE Select ENSP00000478561.1:p.Arg79AlafsTer?
ENST00000490576.1:c.231_232del ENSP00000478839.1:p.Arg79AlafsTer?
ENST00000494864.1:c.-70-3848_-70-3847del ENSP00000479876.1:n.-70-3848_-70-3847del
ENST00000610745.4:c.231_232del ENSP00000478561.1:p.Arg79AlafsTer?
ENST00000613082.1:n.375+622_375+623del
ENST00000614273.1:c.231_232del ENSP00000483678.1:p.Arg79AlafsTer?
NM_000104.3:c.231_232del NP_000095.2:p.Arg79AlafsTer?
NM_000104.4:c.231_232del MANE Select NP_000095.2:p.Arg79AlafsTer?