Canonical Allele Identifier: CA715671396
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs150722579
gnomAD v3: 15-74755380-AC-A
gnomAD v4: 15-74755380-AC-A
MyVariant Identifiers: chr15:g.75047722del (hg19) chr15:g.74755381del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755382del , CM000677.2:g.74755382del GRCh38
NC_000015.9:g.75047723del , CM000677.1:g.75047723del GRCh37
NC_000015.8:g.72834776del NCBI36
NG_008431.1:g.37841del
NG_008431.2:g.37841del
NG_061543.1:g.11538del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*294del MANE Select ENSP00000342007.4:n.*294del
ENST00000343932.4:c.*294del ENSP00000342007.4:n.*294del
NM_000761.4:c.*294del NP_000752.2:n.*294del
NM_000761.5:c.*294del MANE Select NP_000752.2:n.*294del
Search 100 bp 5'
Search 100 bp 3'