Canonical Allele Identifier: CA619123142
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1420935939
gnomAD v2: 15-75047700-AAAC-A
gnomAD v3: 15-74755359-AAAC-A
gnomAD v4: 15-74755359-AAAC-A
MyVariant Identifiers: chr15:g.75047701_75047703del (hg19) chr15:g.74755360_74755362del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755362_74755364del , CM000677.2:g.74755362_74755364del GRCh38
NC_000015.9:g.75047703_75047705del , CM000677.1:g.75047703_75047705del GRCh37
NC_000015.8:g.72834756_72834758del NCBI36
NG_008431.1:g.37821_37823del
NG_008431.2:g.37821_37823del
NG_061543.1:g.11518_11520del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*274_*276del MANE Select ENSP00000342007.4:n.*274_*276del
ENST00000343932.4:c.*274_*276del ENSP00000342007.4:n.*274_*276del
NM_000761.4:c.*274_*276del NP_000752.2:n.*274_*276del
NM_000761.5:c.*274_*276del MANE Select NP_000752.2:n.*274_*276del
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Search 100 bp 3'