Canonical Allele Identifier: CA619412651
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1025609067
gnomAD v2: 15-75047642-C-CA
gnomAD v3: 15-74755301-C-CA
gnomAD v4: 15-74755301-C-CA
MyVariant Identifiers: chr15:g.75047643_75047644insA (hg19) chr15:g.75047642_75047643insA (hg19) chr15:g.74755302_74755303insA (hg38) chr15:g.74755301_74755302insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755311dup , CM000677.2:g.74755311dup GRCh38
NC_000015.9:g.75047652dup , CM000677.1:g.75047652dup GRCh37
NC_000015.8:g.72834705dup NCBI36
NG_008431.1:g.37770dup
NG_008431.2:g.37770dup
NG_061543.1:g.11467dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*223dup MANE Select ENSP00000342007.4:n.*223dup
ENST00000343932.4:c.*223dup ENSP00000342007.4:n.*223dup
NM_000761.4:c.*223dup NP_000752.2:n.*223dup
NM_000761.5:c.*223dup MANE Select NP_000752.2:n.*223dup
Search 100 bp 5'
Search 100 bp 3'