Canonical Allele Identifier: CA2658667384
Gene: CYP1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38074858_38074859del , CM000664.2:g.38074858_38074859del GRCh38
NC_000002.11:g.38302001_38302002del , CM000664.1:g.38302001_38302002del GRCh37
NC_000002.10:g.38155505_38155506del NCBI36
NG_008386.2:g.6243_6244del

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.530_531del ENSP00000478839.2:p.Leu177ArgfsTer?
ENST00000610745.5:c.530_531del MANE Select ENSP00000478561.1:p.Leu177ArgfsTer?
ENST00000494864.1:c.-70-3549_-70-3548del ENSP00000479876.1:n.-70-3549_-70-3548del
ENST00000610745.4:c.530_531del ENSP00000478561.1:p.Leu177ArgfsTer?
ENST00000613082.1:n.376-451_376-450del
ENST00000614273.1:c.530_531del ENSP00000483678.1:p.Leu177ArgfsTer?
NM_000104.3:c.530_531del NP_000095.2:p.Leu177ArgfsTer?
NM_000104.4:c.530_531del MANE Select NP_000095.2:p.Leu177ArgfsTer?