Canonical Allele Identifier: CA971498326
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs2063304339
gnomAD v3: 15-74749664-G-A
gnomAD v4: 15-74749664-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749664G>A , CM000677.2:g.74749664G>A GRCh38
NC_000015.9:g.75042005G>A , CM000677.1:g.75042005G>A GRCh37
NC_000015.8:g.72829058G>A NCBI36
NG_008431.1:g.32123G>A
NG_008431.2:g.32123G>A
NG_061543.1:g.5820G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-66G>A MANE Select ENSP00000342007.4:n.-9-66G>A
ENST00000343932.4:c.-9-66G>A ENSP00000342007.4:n.-9-66G>A
NM_000761.4:c.-9-66G>A NP_000752.2:n.-9-66G>A
NM_000761.5:c.-9-66G>A MANE Select NP_000752.2:n.-9-66G>A
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