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Canonical Allele Identifier:
CA719048474
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.2199375T>C
GRCh37
chr16:g.2249376T>C
Linked Data - NCBI & NCI
dbSNP:
26868
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.2199375T>C , CM000678.2:g.2199375T>C
GRCh38
NC_000016.9:g.2249376T>C , CM000678.1:g.2249376T>C
GRCh37
NC_000016.8:g.2189377T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'