Canonical Allele Identifier: CA2695200450
Gene: CYP1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2637448

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075083_38075112delinsCC , CM000664.2:g.38075083_38075112delinsCC GRCh38
NC_000002.11:g.38302226_38302255delinsCC , CM000664.1:g.38302226_38302255delinsCC GRCh37
NC_000002.10:g.38155730_38155759delinsCC NCBI36
NG_008386.2:g.5990_6019delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.277_306delinsGG ENSP00000478839.2:p.Pro93GlyfsTer?
ENST00000610745.5:c.277_306delinsGG MANE Select ENSP00000478561.1:p.Pro93GlyfsTer?
ENST00000490576.1:c.277_306delinsGG ENSP00000478839.1:p.Pro93GlyfsTer?
ENST00000494864.1:c.-70-3802_-70-3773delinsGG ENSP00000479876.1:n.-70-3802_-70-3773delinsGG
ENST00000610745.4:c.277_306delinsGG ENSP00000478561.1:p.Pro93GlyfsTer?
ENST00000613082.1:n.375+668_376-675delinsGG
ENST00000614273.1:c.277_306delinsGG ENSP00000483678.1:p.Pro93GlyfsTer?
NM_000104.3:c.277_306delinsGG NP_000095.2:p.Pro93GlyfsTer?
NM_000104.4:c.277_306delinsGG MANE Select NP_000095.2:p.Pro93GlyfsTer?