Canonical Allele Identifier: CA1029495296
Gene: CYP1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1682537225
gnomAD v3: 2-38076198-G-A
gnomAD v4: 2-38076198-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38076198G>A , CM000664.2:g.38076198G>A GRCh38
NC_000002.11:g.38303340G>A , CM000664.1:g.38303340G>A GRCh37
NC_000002.10:g.38156844G>A NCBI36
NG_008386.2:g.4904C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000494864.1:c.-70-4888C>T ENSP00000479876.1:n.-70-4888C>T
XM_011533236.1:c.812G>A XP_011531538.1:p.Gly271Glu
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