Canonical Allele Identifier: CA1029495185
Gene: CYP1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1682514382

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075238del , CM000664.2:g.38075238del GRCh38
NC_000002.11:g.38302381del , CM000664.1:g.38302381del GRCh37
NC_000002.10:g.38155885del NCBI36
NG_008386.2:g.5868del

Transcript Alleles

HGVS Amino-acid change
ENST00000490576.2:c.155del ENSP00000478839.2:p.Pro52ArgfsTer8
ENST00000610745.5:c.155del MANE Select ENSP00000478561.1:p.Pro52ArgfsTer8
ENST00000490576.1:c.155del ENSP00000478839.1:p.Pro52ArgfsTer8
ENST00000494864.1:c.-70-3924del ENSP00000479876.1:n.-70-3924del
ENST00000610745.4:c.155del ENSP00000478561.1:p.Pro52ArgfsTer8
ENST00000613082.1:n.375+546del
ENST00000614273.1:c.155del ENSP00000483678.1:p.Pro52ArgfsTer8
NM_000104.3:c.155del NP_000095.2:p.Pro52ArgfsTer8
NM_000104.4:c.155del MANE Select NP_000095.2:p.Pro52ArgfsTer8