Canonical Allele Identifier: CA1245628908
Gene: CYP1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1682542248
gnomAD v4: 2-38076418-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38076418T>A , CM000664.2:g.38076418T>A GRCh38
NC_000002.11:g.38303560T>A , CM000664.1:g.38303560T>A GRCh37
NC_000002.10:g.38157064T>A NCBI36
NG_008386.2:g.4684A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000494864.1:c.-70-5108A>T ENSP00000479876.1:n.-70-5108A>T
XM_011533236.1:c.1032T>A XP_011531538.1:p.Ala344=
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