Canonical Allele Identifier: CA619122997
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1170224806
gnomAD v2: 15-75046947-AAAAAAAAAG-A
gnomAD v3: 15-74754606-AAAAAAAAAG-A
gnomAD v4: 15-74754606-AAAAAAAAAG-A
MyVariant Identifiers: chr15:g.75046948_75046956del (hg19) chr15:g.74754607_74754615del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754610_74754618del , CM000677.2:g.74754610_74754618del GRCh38
NC_000015.9:g.75046951_75046959del , CM000677.1:g.75046951_75046959del GRCh37
NC_000015.8:g.72834004_72834012del NCBI36
NG_008431.1:g.37069_37077del
NG_008431.2:g.37069_37077del
NG_061543.1:g.10766_10774del

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1254-181_1254-173del MANE Select ENSP00000342007.4:n.1254-181_1254-173del
ENST00000343932.4:c.1254-181_1254-173del ENSP00000342007.4:n.1254-181_1254-173del
NM_000761.4:c.1254-181_1254-173del NP_000752.2:n.1254-181_1254-173del
NM_000761.5:c.1254-181_1254-173del MANE Select NP_000752.2:n.1254-181_1254-173del
Search 100 bp 5'
Search 100 bp 3'