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Canonical Allele Identifier:
CA131518821
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.165636879G>A
GRCh37
chr5:g.165063884G>A
Linked Data - Sequence & Population
gnomAD v2:
5:165063884 G / A
gnomAD v3:
5:165636879 G / A
gnomAD v4:
chr5-165636879-G-A
Joint Max Group AF
0.80836598 (EAS)
Genomes Max Group AF
0.80836598 (EAS)
Linked Data - NCBI & NCI
dbSNP:
958994
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.165636879G>A , CM000667.2:g.165636879G>A
GRCh38
NC_000005.9:g.165063884G>A , CM000667.1:g.165063884G>A
GRCh37
NC_000005.8:g.164996462G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'