Canonical Allele Identifier: CA2658667726
Gene: CYP1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38071113dup , CM000664.2:g.38071113dup GRCh38
NC_000002.11:g.38298256dup , CM000664.1:g.38298256dup GRCh37
NC_000002.10:g.38151760dup NCBI36
NG_008386.2:g.9990dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.1242dup ENSP00000478839.2:p.Pro415SerfsTer16
ENST00000610745.5:c.1242dup MANE Select ENSP00000478561.1:p.Pro415SerfsTer16
ENST00000492443.1:n.620dup
ENST00000494864.1:c.129dup ENSP00000479876.1:p.Pro44SerfsTer16
ENST00000610745.4:c.1242dup ENSP00000478561.1:p.Pro415SerfsTer16
ENST00000614273.1:c.1242dup ENSP00000483678.1:p.Pro415SerfsTer16
NM_000104.3:c.1242dup NP_000095.2:p.Pro415SerfsTer16
NM_000104.4:c.1242dup MANE Select NP_000095.2:p.Pro415SerfsTer16