Canonical Allele Identifier: CA619122958
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs61283447
gnomAD v2: 15-75046768-C-CA
gnomAD v3: 15-74754427-C-CA
gnomAD v4: 15-74754427-C-CA
MyVariant Identifiers: chr15:g.75046769_75046770insA (hg19) chr15:g.75046768_75046769insA (hg19) chr15:g.74754428_74754429insA (hg38) chr15:g.74754427_74754428insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754448dup , CM000677.2:g.74754448dup GRCh38
NC_000015.9:g.75046789dup , CM000677.1:g.75046789dup GRCh37
NC_000015.8:g.72833842dup NCBI36
NG_008431.1:g.36907dup
NG_008431.2:g.36907dup
NG_061543.1:g.10604dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1254-343dup MANE Select ENSP00000342007.4:n.1254-343dup
ENST00000343932.4:c.1254-343dup ENSP00000342007.4:n.1254-343dup
NM_000761.4:c.1254-343dup NP_000752.2:n.1254-343dup
NM_000761.5:c.1254-343dup MANE Select NP_000752.2:n.1254-343dup
Search 100 bp 5'
Search 100 bp 3'