ClinGen Allele Registry
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Canonical Allele Identifier:
CA721998895
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.56960218T>C
GRCh37
chr16:g.56994130T>C
Linked Data - NCBI & NCI
dbSNP:
1481328042
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.56960218T>C , CM000678.2:g.56960218T>C
GRCh38
NC_000016.9:g.56994130T>C , CM000678.1:g.56994130T>C
GRCh37
NC_000016.8:g.55551631T>C
NCBI36
NG_008952.1:g.3296T>C
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