Canonical Allele Identifier: CA715672293
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1178749917
gnomAD v3: 15-74749715-CT-C
gnomAD v4: 15-74749715-CT-C
MyVariant Identifiers: chr15:g.75042057del (hg19) chr15:g.74749716del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749721del , CM000677.2:g.74749721del GRCh38
NC_000015.9:g.75042062del , CM000677.1:g.75042062del GRCh37
NC_000015.8:g.72829115del NCBI36
NG_008431.1:g.32180del
NG_008431.2:g.32180del
NG_061543.1:g.5877del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.-9-9del MANE Select ENSP00000342007.4:n.-9-9del
ENST00000343932.4:c.-9-9del ENSP00000342007.4:n.-9-9del
NM_000761.4:c.-9-9del NP_000752.2:n.-9-9del
NM_000761.5:c.-9-9del MANE Select NP_000752.2:n.-9-9del
Search 100 bp 5'
Search 100 bp 3'