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Canonical Allele Identifier:
CA261236089
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.49484632T>C
GRCh37
chr14:g.49951350T>C
Linked Data - Sequence & Population
gnomAD v2:
14:49951350 T / C
gnomAD v3:
14:49484632 T / C
gnomAD v4:
chr14-49484632-T-C
Joint Max Group AF
0.19114451 (NFE)
Genomes Max Group AF
0.19114451 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1530947
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.49484632T>C , CM000676.2:g.49484632T>C
GRCh38
NC_000014.8:g.49951350T>C , CM000676.1:g.49951350T>C
GRCh37
NC_000014.7:g.49021100T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'