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Canonical Allele Identifier:
CA13959812
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.53960339T>G
GRCh37
chr14:g.54427057T>G
Linked Data - Sequence & Population
gnomAD v2:
14:54427057 T / G
gnomAD v3:
14:53960339 T / G
gnomAD v4:
chr14-53960339-T-G
Joint Max Group AF
0.49784526 (EAS)
Genomes Max Group AF
0.49784526 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4898820
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.53960339T>G , CM000676.2:g.53960339T>G
GRCh38
NC_000014.8:g.54427057T>G , CM000676.1:g.54427057T>G
GRCh37
NC_000014.7:g.53496807T>G
NCBI36
NG_009215.1:g.1498A>C
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