Canonical Allele Identifier: CA715670187
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs61283447
gnomAD v3: 15-74754427-CAA-C
gnomAD v4: 15-74754427-CAA-C
MyVariant Identifiers: chr15:g.75046769_75046770del (hg19) chr15:g.74754428_74754429del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754447_74754448del , CM000677.2:g.74754447_74754448del GRCh38
NC_000015.9:g.75046788_75046789del , CM000677.1:g.75046788_75046789del GRCh37
NC_000015.8:g.72833841_72833842del NCBI36
NG_008431.1:g.36906_36907del
NG_008431.2:g.36906_36907del
NG_061543.1:g.10603_10604del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1254-344_1254-343del MANE Select ENSP00000342007.4:n.1254-344_1254-343del
ENST00000343932.4:c.1254-344_1254-343del ENSP00000342007.4:n.1254-344_1254-343del
NM_000761.4:c.1254-344_1254-343del NP_000752.2:n.1254-344_1254-343del
NM_000761.5:c.1254-344_1254-343del MANE Select NP_000752.2:n.1254-344_1254-343del
Search 100 bp 5'
Search 100 bp 3'