Canonical Allele Identifier: CA715670322
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1161571307
gnomAD v3: 15-74754611-AAAAG-A
gnomAD v4: 15-74754611-AAAAG-A
MyVariant Identifiers: chr15:g.75046953_75046956del (hg19) chr15:g.74754612_74754615del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754619_74754622del , CM000677.2:g.74754619_74754622del GRCh38
NC_000015.9:g.75046960_75046963del , CM000677.1:g.75046960_75046963del GRCh37
NC_000015.8:g.72834013_72834016del NCBI36
NG_008431.1:g.37078_37081del
NG_008431.2:g.37078_37081del
NG_061543.1:g.10775_10778del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1254-172_1254-169del MANE Select ENSP00000342007.4:n.1254-172_1254-169del
ENST00000343932.4:c.1254-172_1254-169del ENSP00000342007.4:n.1254-172_1254-169del
NM_000761.4:c.1254-172_1254-169del NP_000752.2:n.1254-172_1254-169del
NM_000761.5:c.1254-172_1254-169del MANE Select NP_000752.2:n.1254-172_1254-169del
Search 100 bp 5'
Search 100 bp 3'