Canonical Allele Identifier: CA619123164
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1041862747
gnomAD v2: 15-75047711-C-CA
gnomAD v3: 15-74755370-C-CA
gnomAD v4: 15-74755370-C-CA
MyVariant Identifiers: chr15:g.75047713_75047714insA (hg19) chr15:g.75047711_75047712insA (hg19) chr15:g.74755372_74755373insA (hg38) chr15:g.74755370_74755371insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755380dup , CM000677.2:g.74755380dup GRCh38
NC_000015.9:g.75047721dup , CM000677.1:g.75047721dup GRCh37
NC_000015.8:g.72834774dup NCBI36
NG_008431.1:g.37839dup
NG_008431.2:g.37839dup
NG_061543.1:g.11536dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*292dup MANE Select ENSP00000342007.4:n.*292dup
ENST00000343932.4:c.*292dup ENSP00000342007.4:n.*292dup
NM_000761.4:c.*292dup NP_000752.2:n.*292dup
NM_000761.5:c.*292dup MANE Select NP_000752.2:n.*292dup
Search 100 bp 5'
Search 100 bp 3'