Canonical Allele Identifier: CA2749546741
Gene: CYP1B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075559_38075564del , CM000664.2:g.38075559_38075564del GRCh38
NC_000002.11:g.38302702_38302707del , CM000664.1:g.38302702_38302707del GRCh37
NC_000002.10:g.38156206_38156211del NCBI36
NG_008386.2:g.5538_5543del

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.-1-175_-1-170del ENSP00000478839.2:n.-1-175_-1-170del
ENST00000610745.5:c.-1-175_-1-170del MANE Select ENSP00000478561.1:n.-1-175_-1-170del
ENST00000490576.1:c.-1-175_-1-170del ENSP00000478839.1:n.-1-175_-1-170del
ENST00000494864.1:c.-70-4254_-70-4249del ENSP00000479876.1:n.-70-4254_-70-4249del
ENST00000610745.4:c.-1-175_-1-170del ENSP00000478561.1:n.-1-175_-1-170del
ENST00000613082.1:n.375+216_375+221del
ENST00000614273.1:c.-1-175_-1-170del ENSP00000483678.1:n.-1-175_-1-170del
NM_000104.3:c.-1-175_-1-170del NP_000095.2:n.-1-175_-1-170del
XM_011533236.1:c.173_178del XP_011531538.1:p.Pro58_Glu60delinsGln
NM_000104.4:c.-1-175_-1-170del MANE Select NP_000095.2:n.-1-175_-1-170del
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