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Canonical Allele Identifier:
CA678623777
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.57595144C>T
GRCh37
chr11:g.57362617C>T
Linked Data - NCBI & NCI
dbSNP:
2509897
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.57595144C>T , CM000673.2:g.57595144C>T
GRCh38
NC_000011.9:g.57362617C>T , CM000673.1:g.57362617C>T
GRCh37
NC_000011.8:g.57119193C>T
NCBI36
NG_009625.1:g.2591C>T , LRG_105:g.2591C>T
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