Canonical Allele Identifier: CA534498880
Gene:

Linked Data

dbSNP Id: rs1217642106
gnomAD v2: 2-88315657-AT-A
gnomAD v3: 2-88016138-AT-A
gnomAD v4: 2-88016138-AT-A
MyVariant Identifiers: chr2:g.88315658del (hg19) chr2:g.88016139del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016139del , CM000664.2:g.88016139del GRCh38
NC_000002.11:g.88315658del , CM000664.1:g.88315658del GRCh37
NC_000002.10:g.88096773del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.484del
XR_940336.3:n.484del
Search 100 bp 5'
Search 100 bp 3'