ClinGen Allele Registry
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Canonical Allele Identifier:
CA760016594
Gene:
Linked Data
dbSNP Id:
rs1237922273
MyVariant Identifiers:
chr2:g.16639398del (hg19)
chr2:g.16458130del (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.16458134del , CM000664.2:g.16458134del
GRCh38
NC_000002.11:g.16639402del , CM000664.1:g.16639402del
GRCh37
NC_000002.10:g.16502883del
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_939752.1:n.396-3036del
Search 100 bp 5'
Search 100 bp 3'