Canonical Allele Identifier: CA272816266
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs922807959
gnomAD v2: 15-75047699-A-AC
gnomAD v3: 15-74755358-A-AC
gnomAD v4: 15-74755358-A-AC
MyVariant Identifiers: chr15:g.75047699_75047700insC (hg19) chr15:g.75047700_75047703delinsCAAAC (hg19) chr15:g.74755358_74755359insC (hg38) chr15:g.74755359_74755362delinsCAAAC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755358_74755359insC , CM000677.2:g.74755358_74755359insC GRCh38
NC_000015.9:g.75047699_75047700insC , CM000677.1:g.75047699_75047700insC GRCh37
NC_000015.8:g.72834752_72834753insC NCBI36
NG_008431.1:g.37817_37818insC
NG_008431.2:g.37817_37818insC
NG_061543.1:g.11514_11515insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*270_*271insC MANE Select ENSP00000342007.4:n.*270_*271insC
ENST00000343932.4:c.*270_*271insC ENSP00000342007.4:n.*270_*271insC
NM_000761.4:c.*270_*271insC NP_000752.2:n.*270_*271insC
NM_000761.5:c.*270_*271insC MANE Select NP_000752.2:n.*270_*271insC
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