ClinGen Allele Registry
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Canonical Allele Identifier:
CA208363497
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.67884201A>T
GRCh37
chr10:g.69643959A>T
Linked Data - NCBI & NCI
dbSNP:
3740051
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.67884201A>T , CM000672.2:g.67884201A>T
GRCh38
NC_000010.10:g.69643959A>T , CM000672.1:g.69643959A>T
GRCh37
NC_000010.9:g.69313965A>T
NCBI36
NG_050664.1:g.4540A>T
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