Canonical Allele Identifier: CA272816296
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs150722579
gnomAD v2: 15-75047721-A-AC
gnomAD v3: 15-74755380-A-AC
gnomAD v4: 15-74755380-A-AC
COSMIC: COSN17873140
MyVariant Identifiers: chr15:g.75047721_75047722insC (hg19) chr15:g.74755380_74755381insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755382dup , CM000677.2:g.74755382dup GRCh38
NC_000015.9:g.75047723dup , CM000677.1:g.75047723dup GRCh37
NC_000015.8:g.72834776dup NCBI36
NG_008431.1:g.37841dup
NG_008431.2:g.37841dup
NG_061543.1:g.11538dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*294dup MANE Select ENSP00000342007.4:n.*294dup
ENST00000343932.4:c.*294dup ENSP00000342007.4:n.*294dup
NM_000761.4:c.*294dup NP_000752.2:n.*294dup
NM_000761.5:c.*294dup MANE Select NP_000752.2:n.*294dup
Search 100 bp 5'
Search 100 bp 3'