Canonical Allele Identifier: CA2698952737
Gene: CYP1B1 HGNC NCBI

Linked Data

dbSNP Id: rs2125316456
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075267del , CM000664.2:g.38075267del GRCh38
NC_000002.11:g.38302410del , CM000664.1:g.38302410del GRCh37
NC_000002.10:g.38155914del NCBI36
NG_008386.2:g.5836del

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.123del ENSP00000478839.2:p.Arg41SerfsTer19
ENST00000610745.5:c.123del MANE Select ENSP00000478561.1:p.Arg41SerfsTer19
ENST00000490576.1:c.123del ENSP00000478839.1:p.Arg41SerfsTer19
ENST00000494864.1:c.-70-3956del ENSP00000479876.1:n.-70-3956del
ENST00000610745.4:c.123del ENSP00000478561.1:p.Arg41SerfsTer19
ENST00000613082.1:n.375+514del
ENST00000614273.1:c.123del ENSP00000483678.1:p.Arg41SerfsTer19
NM_000104.3:c.123del NP_000095.2:p.Arg41SerfsTer19
NM_000104.4:c.123del MANE Select NP_000095.2:p.Arg41SerfsTer19
Search 100 bp 5'
Search 100 bp 3'