Canonical Allele Identifier: CA7659682
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs758752876
ExAC: 15:75042179 CG / C
gnomAD v2: 15-75042179-CG-C
gnomAD v3: 15-74749838-CG-C
gnomAD v4: 15-74749838-CG-C
MyVariant Identifiers: chr15:g.75042180del (hg19) chr15:g.74749839del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749841del , CM000677.2:g.74749841del GRCh38
NC_000015.9:g.75042182del , CM000677.1:g.75042182del GRCh37
NC_000015.8:g.72829235del NCBI36
NG_008431.1:g.32300del
NG_008431.2:g.32300del
NG_061543.1:g.5997del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.103del MANE Select ENSP00000342007.4:p.Val35SerfsTer5
ENST00000343932.4:c.103del ENSP00000342007.4:p.Val35SerfsTer5
NM_000761.4:c.103del NP_000752.2:p.Val35SerfsTer5
NM_000761.5:c.103del MANE Select NP_000752.2:p.Val35SerfsTer5
Search 100 bp 5'
Search 100 bp 3'