ClinGen Allele Registry
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Canonical Allele Identifier:
CA726247021
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.13636487T>A
GRCh37
chr17:g.13539804T>A
Linked Data - NCBI & NCI
dbSNP:
10521232
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.13636487T>A , CM000679.2:g.13636487T>A
GRCh38
NC_000017.10:g.13539804T>A , CM000679.1:g.13539804T>A
GRCh37
NC_000017.9:g.13480529T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'