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Canonical Allele Identifier:
CA679144860
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.636689G>T
GRCh37
chr11:g.636689G>T
Linked Data - NCBI & NCI
dbSNP:
747302
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.636689G>T , CM000673.2:g.636689G>T
GRCh38
NC_000011.9:g.636689G>T , CM000673.1:g.636689G>T
GRCh37
NC_000011.8:g.626689G>T
NCBI36
NG_021241.1:g.4385G>T
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