ClinGen Allele Registry
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Canonical Allele Identifier:
CA262598261
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.73136289G>A
GRCh37
chr14:g.73602997G>A
Linked Data - Sequence & Population
gnomAD v2:
14:73602997 G / A
gnomAD v3:
14:73136289 G / A
gnomAD v4:
chr14-73136289-G-A
Joint Max Group AF
0.00018175 (NFE)
Genomes Max Group AF
0.00018203 (NFE)
Linked Data - NCBI & NCI
dbSNP:
780591217
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.73136289G>A , CM000676.2:g.73136289G>A
GRCh38
NC_000014.8:g.73602997G>A , CM000676.1:g.73602997G>A
GRCh37
NC_000014.7:g.72672750G>A
NCBI36
NG_007386.2:g.4819G>A
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