Canonical Allele Identifier: CA2586969067
Gene: CYP1B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38071145_38071156dup , CM000664.2:g.38071145_38071156dup GRCh38
NC_000002.11:g.38298288_38298299dup , CM000664.1:g.38298288_38298299dup GRCh37
NC_000002.10:g.38151792_38151803dup NCBI36
NG_008386.2:g.9946_9957dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.1198_1209dup ENSP00000478839.2:p.Thr403_Thr404insProHisAlaThr
ENST00000610745.5:c.1198_1209dup MANE Select ENSP00000478561.1:p.Thr403_Thr404insProHisAlaThr
ENST00000492443.1:n.576_587dup
ENST00000494864.1:c.85_96dup ENSP00000479876.1:p.Thr32_Thr33insProHisAlaThr
ENST00000610745.4:c.1198_1209dup ENSP00000478561.1:p.Thr403_Thr404insProHisAlaThr
ENST00000614273.1:c.1198_1209dup ENSP00000483678.1:p.Thr403_Thr404insProHisAlaThr
NM_000104.3:c.1198_1209dup NP_000095.2:p.Thr403_Thr404insProHisAlaThr
NM_000104.4:c.1198_1209dup MANE Select NP_000095.2:p.Thr403_Thr404insProHisAlaThr
Search 100 bp 5'
Search 100 bp 3'