Canonical Allele Identifier: CA971501157
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs2063333912
gnomAD v3: 15-74755380-A-AAC
gnomAD v4: 15-74755380-A-AAC
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755380_74755381insAC , CM000677.2:g.74755380_74755381insAC GRCh38
NC_000015.9:g.75047721_75047722insAC , CM000677.1:g.75047721_75047722insAC GRCh37
NC_000015.8:g.72834774_72834775insAC NCBI36
NG_008431.1:g.37839_37840insAC
NG_008431.2:g.37839_37840insAC
NG_061543.1:g.11536_11537insAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*292_*293insAC MANE Select ENSP00000342007.4:n.*292_*293insAC
ENST00000343932.4:c.*292_*293insAC ENSP00000342007.4:n.*292_*293insAC
NM_000761.4:c.*292_*293insAC NP_000752.2:n.*292_*293insAC
NM_000761.5:c.*292_*293insAC MANE Select NP_000752.2:n.*292_*293insAC
Search 100 bp 5'
Search 100 bp 3'