Canonical Allele Identifier: CA272816287
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs535172419
gnomAD v2: 15-75047714-A-AC
gnomAD v3: 15-74755373-A-AC
gnomAD v4: 15-74755373-A-AC
MyVariant Identifiers: chr15:g.75047714_75047715insC (hg19) chr15:g.74755373_74755374insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755373_74755374insC , CM000677.2:g.74755373_74755374insC GRCh38
NC_000015.9:g.75047714_75047715insC , CM000677.1:g.75047714_75047715insC GRCh37
NC_000015.8:g.72834767_72834768insC NCBI36
NG_008431.1:g.37832_37833insC
NG_008431.2:g.37832_37833insC
NG_061543.1:g.11529_11530insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*285_*286insC MANE Select ENSP00000342007.4:n.*285_*286insC
ENST00000343932.4:c.*285_*286insC ENSP00000342007.4:n.*285_*286insC
NM_000761.4:c.*285_*286insC NP_000752.2:n.*285_*286insC
NM_000761.5:c.*285_*286insC MANE Select NP_000752.2:n.*285_*286insC
Search 100 bp 5'
Search 100 bp 3'