Canonical Allele Identifier: CA619123154
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1358442567
gnomAD v2: 15-75047707-C-CA
gnomAD v3: 15-74755366-C-CA
gnomAD v4: 15-74755366-C-CA
MyVariant Identifiers: chr15:g.75047707_75047708insA (hg19) chr15:g.74755366_74755367insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755369dup , CM000677.2:g.74755369dup GRCh38
NC_000015.9:g.75047710dup , CM000677.1:g.75047710dup GRCh37
NC_000015.8:g.72834763dup NCBI36
NG_008431.1:g.37828dup
NG_008431.2:g.37828dup
NG_061543.1:g.11525dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*281dup MANE Select ENSP00000342007.4:n.*281dup
ENST00000343932.4:c.*281dup ENSP00000342007.4:n.*281dup
NM_000761.4:c.*281dup NP_000752.2:n.*281dup
NM_000761.5:c.*281dup MANE Select NP_000752.2:n.*281dup
Search 100 bp 5'
Search 100 bp 3'