Canonical Allele Identifier: CA7660058
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs780344039
ExAC: 15:75047146 AC / A
gnomAD v2: 15-75047146-AC-A
gnomAD v4: 15-74754805-AC-A
MyVariant Identifiers: chr15:g.75047147del (hg19) chr15:g.74754806del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754809del , CM000677.2:g.74754809del GRCh38
NC_000015.9:g.75047150del , CM000677.1:g.75047150del GRCh37
NC_000015.8:g.72834203del NCBI36
NG_008431.1:g.37268del
NG_008431.2:g.37268del
NG_061543.1:g.10965del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1272del MANE Select ENSP00000342007.4:p.Ser425LeufsTer20
ENST00000343932.4:c.1272del ENSP00000342007.4:p.Ser425LeufsTer20
NM_000761.4:c.1272del NP_000752.2:p.Ser425LeufsTer20
NM_000761.5:c.1272del MANE Select NP_000752.2:p.Ser425LeufsTer20
Search 100 bp 5'
Search 100 bp 3'