Canonical Allele Identifier: CA2658667813
Gene: CYP1B1 HGNC NCBI

Linked Data

gnomAD v4: 2-38075476-T-TAG
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075476_38075477insAG , CM000664.2:g.38075476_38075477insAG GRCh38
NC_000002.11:g.38302619_38302620insAG , CM000664.1:g.38302619_38302620insAG GRCh37
NC_000002.10:g.38156123_38156124insAG NCBI36
NG_008386.2:g.5625_5626insCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.-1-88_-1-87insCT ENSP00000478839.2:n.-1-88_-1-87insCT
ENST00000610745.5:c.-1-88_-1-87insCT MANE Select ENSP00000478561.1:n.-1-88_-1-87insCT
ENST00000490576.1:c.-1-88_-1-87insCT ENSP00000478839.1:n.-1-88_-1-87insCT
ENST00000494864.1:c.-70-4167_-70-4166insCT ENSP00000479876.1:n.-70-4167_-70-4166insCT
ENST00000610745.4:c.-1-88_-1-87insCT ENSP00000478561.1:n.-1-88_-1-87insCT
ENST00000613082.1:n.375+303_375+304insCT
ENST00000614273.1:c.-1-88_-1-87insCT ENSP00000483678.1:n.-1-88_-1-87insCT
NM_000104.3:c.-1-88_-1-87insCT NP_000095.2:n.-1-88_-1-87insCT
XM_011533236.1:c.90_91insAG XP_011531538.1:p.Glu31ArgfsTer11
NM_000104.4:c.-1-88_-1-87insCT MANE Select NP_000095.2:n.-1-88_-1-87insCT
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