Canonical Allele Identifier: CA2658668322
Gene: CYP1B1 HGNC NCBI

Linked Data

gnomAD v4: 2-38076312-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38076312A>G , CM000664.2:g.38076312A>G GRCh38
NC_000002.11:g.38303454A>G , CM000664.1:g.38303454A>G GRCh37
NC_000002.10:g.38156958A>G NCBI36
NG_008386.2:g.4790T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000494864.1:c.-70-5002T>C ENSP00000479876.1:n.-70-5002T>C
XM_011533236.1:c.926A>G XP_011531538.1:p.Gln309Arg
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