ClinGen Allele Registry
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Canonical Allele Identifier:
CA773789667
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.61419916A>T
GRCh37
chr17:g.59497277A>T
Linked Data - NCBI & NCI
dbSNP:
757608
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.61419916A>T , CM000679.2:g.61419916A>T
GRCh38
NC_000017.10:g.59497277A>T , CM000679.1:g.59497277A>T
GRCh37
NC_000017.9:g.56852059A>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'