Canonical Allele Identifier: CA2658668220
Gene: CYP1B1 HGNC NCBI

Linked Data

gnomAD v4: 2-38076221-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38076221C>A , CM000664.2:g.38076221C>A GRCh38
NC_000002.11:g.38303363C>A , CM000664.1:g.38303363C>A GRCh37
NC_000002.10:g.38156867C>A NCBI36
NG_008386.2:g.4881G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000494864.1:c.-70-4911G>T ENSP00000479876.1:n.-70-4911G>T
XM_011533236.1:c.835C>A XP_011531538.1:p.Arg279=
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