ClinGen Allele Registry
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Canonical Allele Identifier:
CA855860438
Gene:
Linked Data
dbSNP Id:
rs1444083615
MyVariant Identifiers:
chr8:g.82390569G>T (hg19)
chr8:g.81478334G>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.81478334G>T , CM000670.2:g.81478334G>T
GRCh38
NC_000008.10:g.82390569G>T , CM000670.1:g.82390569G>T
GRCh37
NC_000008.9:g.82553124G>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001745980.1:n.514+16360G>T
Search 100 bp 5'
Search 100 bp 3'