Canonical Allele Identifier: CA2658667739
Gene: CYP1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38071272_38071278dup , CM000664.2:g.38071272_38071278dup GRCh38
NC_000002.11:g.38298415_38298421dup , CM000664.1:g.38298415_38298421dup GRCh37
NC_000002.10:g.38151919_38151925dup NCBI36
NG_008386.2:g.9824_9830dup

Transcript Alleles

HGVS Amino-acid change
ENST00000490576.2:c.1076_1082dup ENSP00000478839.2:p.Asp361GlufsTer16
ENST00000610745.5:c.1076_1082dup MANE Select ENSP00000478561.1:p.Asp361GlufsTer16
ENST00000492443.1:n.454_460dup
ENST00000494864.1:c.-38_-32dup ENSP00000479876.1:n.-38_-32dup
ENST00000610745.4:c.1076_1082dup ENSP00000478561.1:p.Asp361GlufsTer16
ENST00000613082.1:n.471_477dup
ENST00000614273.1:c.1076_1082dup ENSP00000483678.1:p.Asp361GlufsTer16
NM_000104.3:c.1076_1082dup NP_000095.2:p.Asp361GlufsTer16
NM_000104.4:c.1076_1082dup MANE Select NP_000095.2:p.Asp361GlufsTer16