Canonical Allele Identifier: CA272815988
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs879367778
gnomAD v2: 15-75046942-CA-C
gnomAD v3: 15-74754601-CA-C
gnomAD v4: 15-74754601-CA-C
MyVariant Identifiers: chr15:g.75046944del (hg19) chr15:g.75046943del (hg19) chr15:g.74754603del (hg38) chr15:g.74754602del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754614del , CM000677.2:g.74754614del GRCh38
NC_000015.9:g.75046955del , CM000677.1:g.75046955del GRCh37
NC_000015.8:g.72834008del NCBI36
NG_008431.1:g.37073del
NG_008431.2:g.37073del
NG_061543.1:g.10770del

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1254-177del MANE Select ENSP00000342007.4:n.1254-177del
ENST00000343932.4:c.1254-177del ENSP00000342007.4:n.1254-177del
NM_000761.4:c.1254-177del NP_000752.2:n.1254-177del
NM_000761.5:c.1254-177del MANE Select NP_000752.2:n.1254-177del
Search 100 bp 5'
Search 100 bp 3'