Canonical Allele Identifier: CA272816277
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs57295890
gnomAD v2: 15-75047710-AC-A
gnomAD v3: 15-74755369-AC-A
gnomAD v4: 15-74755369-AC-A
MyVariant Identifiers: chr15:g.75047711del (hg19) chr15:g.74755370del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755370del , CM000677.2:g.74755370del GRCh38
NC_000015.9:g.75047711del , CM000677.1:g.75047711del GRCh37
NC_000015.8:g.72834764del NCBI36
NG_008431.1:g.37829del
NG_008431.2:g.37829del
NG_061543.1:g.11526del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*282del MANE Select ENSP00000342007.4:n.*282del
ENST00000343932.4:c.*282del ENSP00000342007.4:n.*282del
NM_000761.4:c.*282del NP_000752.2:n.*282del
NM_000761.5:c.*282del MANE Select NP_000752.2:n.*282del
Search 100 bp 5'
Search 100 bp 3'