ClinGen Allele Registry
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Canonical Allele Identifier:
CA846959239
Gene:
Linked Data
dbSNP Id:
rs1251260204
MyVariant Identifiers:
chr8:g.126490976A>G (hg19)
chr8:g.125478734A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.125478734A>G , CM000670.2:g.125478734A>G
GRCh38
NC_000008.10:g.126490976A>G , CM000670.1:g.126490976A>G
GRCh37
NC_000008.9:g.126560158A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_928628.1:n.256+5420A>G
Search 100 bp 5'
Search 100 bp 3'