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Canonical Allele Identifier:
CA256493502
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.105545945G>T
GRCh37
chr13:g.106198294G>T
Linked Data - NCBI & NCI
dbSNP:
758593897
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.105545945G>T , CM000675.2:g.105545945G>T
GRCh38
NC_000013.10:g.106198294G>T , CM000675.1:g.106198294G>T
GRCh37
NC_000013.9:g.104996295G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'