Canonical Allele Identifier: CA2658668443
Gene: CYP1B1 HGNC NCBI

Linked Data

gnomAD v4: 2-38076415-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38076415C>A , CM000664.2:g.38076415C>A GRCh38
NC_000002.11:g.38303557C>A , CM000664.1:g.38303557C>A GRCh37
NC_000002.10:g.38157061C>A NCBI36
NG_008386.2:g.4687G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000494864.1:c.-70-5105G>T ENSP00000479876.1:n.-70-5105G>T
XM_011533236.1:c.1029C>A XP_011531538.1:p.His343Gln
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