Canonical Allele Identifier: CA2658667722
Gene: CYP1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075112_38075113del , CM000664.2:g.38075112_38075113del GRCh38
NC_000002.11:g.38302255_38302256del , CM000664.1:g.38302255_38302256del GRCh37
NC_000002.10:g.38155759_38155760del NCBI36
NG_008386.2:g.5991_5992del

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.278_279del ENSP00000478839.2:p.Pro93HisfsTer?
ENST00000610745.5:c.278_279del MANE Select ENSP00000478561.1:p.Pro93HisfsTer?
ENST00000490576.1:c.278_279del ENSP00000478839.1:p.Pro93HisfsTer?
ENST00000494864.1:c.-70-3801_-70-3800del ENSP00000479876.1:n.-70-3801_-70-3800del
ENST00000610745.4:c.278_279del ENSP00000478561.1:p.Pro93HisfsTer?
ENST00000613082.1:n.375+669_375+670del
ENST00000614273.1:c.278_279del ENSP00000483678.1:p.Pro93HisfsTer?
NM_000104.3:c.278_279del NP_000095.2:p.Pro93HisfsTer?
NM_000104.4:c.278_279del MANE Select NP_000095.2:p.Pro93HisfsTer?