ClinGen Allele Registry
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Canonical Allele Identifier:
CA262598333
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.73136382C>A
GRCh37
chr14:g.73603090C>A
Linked Data - Sequence & Population
gnomAD v3:
14:73136382 C / A
gnomAD v4:
chr14-73136382-C-A
Joint Max Group AF
0.00002259 (AMR)
Genomes Max Group AF
0.0000226 (AMR)
Linked Data - NCBI & NCI
dbSNP:
972605327
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.73136382C>A , CM000676.2:g.73136382C>A
GRCh38
NC_000014.8:g.73603090C>A , CM000676.1:g.73603090C>A
GRCh37
NC_000014.7:g.72672843C>A
NCBI36
NG_007386.2:g.4912C>A
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