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Canonical Allele Identifier:
CA895917444
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.97711412A>T
GRCh37
chr2:g.98327875A>T
Linked Data - NCBI & NCI
dbSNP:
17695937
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.97711412A>T , CM000664.2:g.97711412A>T
GRCh38
NC_000002.11:g.98327875A>T , CM000664.1:g.98327875A>T
GRCh37
NC_000002.10:g.97694307A>T
NCBI36
NG_007727.1:g.2845A>T , LRG_126:g.2845A>T
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