Canonical Allele Identifier: CA715671345
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1165365847
gnomAD v3: 15-74755366-CAAACA-C
gnomAD v4: 15-74755366-CAAACA-C
MyVariant Identifiers: chr15:g.75047708_75047712del (hg19) chr15:g.74755367_74755371del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755370_74755374del , CM000677.2:g.74755370_74755374del GRCh38
NC_000015.9:g.75047711_75047715del , CM000677.1:g.75047711_75047715del GRCh37
NC_000015.8:g.72834764_72834768del NCBI36
NG_008431.1:g.37829_37833del
NG_008431.2:g.37829_37833del
NG_061543.1:g.11526_11530del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*282_*286del MANE Select ENSP00000342007.4:n.*282_*286del
ENST00000343932.4:c.*282_*286del ENSP00000342007.4:n.*282_*286del
NM_000761.4:c.*282_*286del NP_000752.2:n.*282_*286del
NM_000761.5:c.*282_*286del MANE Select NP_000752.2:n.*282_*286del
Search 100 bp 5'
Search 100 bp 3'