Canonical Allele Identifier: CA1245628264
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075233_38075234delinsCG , CM000664.2:g.38075233_38075234delinsCG GRCh38
NC_000002.11:g.38302376_38302377delinsCG , CM000664.1:g.38302376_38302377delinsCG GRCh37
NC_000002.10:g.38155880_38155881delinsCG NCBI36
NG_008386.2:g.5868_5869delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000490576.2:c.155_156delinsCG ENSP00000478839.2:p.Pro52=
ENST00000610745.5:c.155_156delinsCG MANE Select ENSP00000478561.1:p.Pro52=
ENST00000490576.1:c.155_156delinsCG ENSP00000478839.1:p.Pro52=
ENST00000494864.1:c.-70-3924_-70-3923delinsCG ENSP00000479876.1:n.-70-3924_-70-3923deli...
ENST00000610745.4:c.155_156delinsCG ENSP00000478561.1:p.Pro52=
ENST00000613082.1:n.375+546_375+547delinsCG
ENST00000614273.1:c.155_156delinsCG ENSP00000483678.1:p.Pro52=
NM_000104.3:c.155_156delinsCG NP_000095.2:p.Pro52=
NM_000104.4:c.155_156delinsCG MANE Select NP_000095.2:p.Pro52=