ClinGen Allele Registry
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Canonical Allele Identifier:
CA712620519
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.38856450G>A
GRCh37
chr15:g.39148651G>A
Linked Data - NCBI & NCI
dbSNP:
1250316669
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.38856450G>A , CM000677.2:g.38856450G>A
GRCh38
NC_000015.9:g.39148651G>A , CM000677.1:g.39148651G>A
GRCh37
NC_000015.8:g.36935943G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'