Canonical Allele Identifier: CA2658668329
Gene: CYP1B1 HGNC NCBI

Linked Data

gnomAD v4: 2-38076320-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38076320T>C , CM000664.2:g.38076320T>C GRCh38
NC_000002.11:g.38303462T>C , CM000664.1:g.38303462T>C GRCh37
NC_000002.10:g.38156966T>C NCBI36
NG_008386.2:g.4782A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000494864.1:c.-70-5010A>G ENSP00000479876.1:n.-70-5010A>G
XM_011533236.1:c.934T>C XP_011531538.1:p.Phe312Leu
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