ClinGen Allele Registry
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Canonical Allele Identifier:
CA181599871
Gene:
Linked Data
dbSNP Id:
rs77905013
MyVariant Identifiers:
chr8:g.89993396A>G (hg19)
chr8:g.88981167A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.88981167A>G , CM000670.2:g.88981167A>G
GRCh38
NC_000008.10:g.89993396A>G , CM000670.1:g.89993396A>G
GRCh37
NC_000008.9:g.90062512A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid change
XR_002956667.1:n.179-99106T>C
Search 100 bp 5'
Search 100 bp 3'