Canonical Allele Identifier: CA619123141
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs200675446
gnomAD v2: 15-75047691-C-CA
gnomAD v3: 15-74755350-C-CA
gnomAD v4: 15-74755350-C-CA
MyVariant Identifiers: chr15:g.75047695_75047696insA (hg19) chr15:g.75047691_75047692insA (hg19) chr15:g.74755354_74755355insA (hg38) chr15:g.74755350_74755351insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755361dup , CM000677.2:g.74755361dup GRCh38
NC_000015.9:g.75047702dup , CM000677.1:g.75047702dup GRCh37
NC_000015.8:g.72834755dup NCBI36
NG_008431.1:g.37820dup
NG_008431.2:g.37820dup
NG_061543.1:g.11517dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*273dup MANE Select ENSP00000342007.4:n.*273dup
ENST00000343932.4:c.*273dup ENSP00000342007.4:n.*273dup
NM_000761.4:c.*273dup NP_000752.2:n.*273dup
NM_000761.5:c.*273dup MANE Select NP_000752.2:n.*273dup
Search 100 bp 5'
Search 100 bp 3'