Canonical Allele Identifier: CA2658668440
Gene: CYP1B1 HGNC NCBI

Linked Data

gnomAD v4: 2-38076413-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38076413C>T , CM000664.2:g.38076413C>T GRCh38
NC_000002.11:g.38303555C>T , CM000664.1:g.38303555C>T GRCh37
NC_000002.10:g.38157059C>T NCBI36
NG_008386.2:g.4689G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000494864.1:c.-70-5103G>A ENSP00000479876.1:n.-70-5103G>A
XM_011533236.1:c.1027C>T XP_011531538.1:p.His343Tyr
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