Canonical Allele Identifier: CA2749546732
Gene: CYP1B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075545_38075567del , CM000664.2:g.38075545_38075567del GRCh38
NC_000002.11:g.38302688_38302710del , CM000664.1:g.38302688_38302710del GRCh37
NC_000002.10:g.38156192_38156214del NCBI36
NG_008386.2:g.5535_5557del

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.-1-178_-1-156del ENSP00000478839.2:n.-1-178_-1-156del
ENST00000610745.5:c.-1-178_-1-156del MANE Select ENSP00000478561.1:n.-1-178_-1-156del
ENST00000490576.1:c.-1-178_-1-156del ENSP00000478839.1:n.-1-178_-1-156del
ENST00000494864.1:c.-70-4257_-70-4235del ENSP00000479876.1:n.-70-4257_-70-4235del
ENST00000610745.4:c.-1-178_-1-156del ENSP00000478561.1:n.-1-178_-1-156del
ENST00000613082.1:n.375+213_375+235del
ENST00000614273.1:c.-1-178_-1-156del ENSP00000483678.1:n.-1-178_-1-156del
NM_000104.3:c.-1-178_-1-156del NP_000095.2:n.-1-178_-1-156del
XM_011533236.1:c.159_181del XP_011531538.1:p.Pro54GlufsTer10
NM_000104.4:c.-1-178_-1-156del MANE Select NP_000095.2:n.-1-178_-1-156del
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