ClinGen Allele Registry
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Canonical Allele Identifier:
CA719894699
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.31096404A>C
GRCh37
chr16:g.31107725A>C
Linked Data - NCBI & NCI
dbSNP:
1274700616
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.31096404A>C , CM000678.2:g.31096404A>C
GRCh38
NC_000016.9:g.31107725A>C , CM000678.1:g.31107725A>C
GRCh37
NC_000016.8:g.31015226A>C
NCBI36
NG_011564.1:g.3552T>G
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