Canonical Allele Identifier: CA619123155
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1387275596
gnomAD v2: 15-75047708-AAAC-A
gnomAD v3: 15-74755367-AAAC-A
gnomAD v4: 15-74755367-AAAC-A
MyVariant Identifiers: chr15:g.75047709_75047711del (hg19) chr15:g.74755368_74755370del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755370_74755372del , CM000677.2:g.74755370_74755372del GRCh38
NC_000015.9:g.75047711_75047713del , CM000677.1:g.75047711_75047713del GRCh37
NC_000015.8:g.72834764_72834766del NCBI36
NG_008431.1:g.37829_37831del
NG_008431.2:g.37829_37831del
NG_061543.1:g.11526_11528del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*282_*284del MANE Select ENSP00000342007.4:n.*282_*284del
ENST00000343932.4:c.*282_*284del ENSP00000342007.4:n.*282_*284del
NM_000761.4:c.*282_*284del NP_000752.2:n.*282_*284del
NM_000761.5:c.*282_*284del MANE Select NP_000752.2:n.*282_*284del
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Search 100 bp 3'