Canonical Allele Identifier: CA619123182
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1226676958
gnomAD v2: 15-75047720-A-AC
gnomAD v3: 15-74755379-A-AC
gnomAD v4: 15-74755379-A-AC
MyVariant Identifiers: chr15:g.75047720_75047721insC (hg19) chr15:g.74755379_74755380insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755379_74755380insC , CM000677.2:g.74755379_74755380insC GRCh38
NC_000015.9:g.75047720_75047721insC , CM000677.1:g.75047720_75047721insC GRCh37
NC_000015.8:g.72834773_72834774insC NCBI36
NG_008431.1:g.37838_37839insC
NG_008431.2:g.37838_37839insC
NG_061543.1:g.11535_11536insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*291_*292insC MANE Select ENSP00000342007.4:n.*291_*292insC
ENST00000343932.4:c.*291_*292insC ENSP00000342007.4:n.*291_*292insC
NM_000761.4:c.*291_*292insC NP_000752.2:n.*291_*292insC
NM_000761.5:c.*291_*292insC MANE Select NP_000752.2:n.*291_*292insC
Search 100 bp 5'
Search 100 bp 3'