ClinGen Allele Registry
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Canonical Allele Identifier:
CA15816419
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.35405064G>A
GRCh37
chr14:g.35874270G>A
Linked Data - Sequence & Population
gnomAD v2:
14:35874270 G / A
gnomAD v3:
14:35405064 G / A
gnomAD v4:
chr14-35405064-G-A
Joint Max Group AF
0.23630428 (NFE)
Genomes Max Group AF
0.23630428 (NFE)
Linked Data - NCBI & NCI
ClinVar RCV:
RCV001517839
RCV001655765
ClinVar Variation:
1167988
dbSNP:
2233409
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.35405064G>A , CM000676.2:g.35405064G>A
GRCh38
NC_000014.8:g.35874270G>A , CM000676.1:g.35874270G>A
GRCh37
NC_000014.7:g.34944021G>A
NCBI36
NG_007571.1:g.4675C>T , LRG_89:g.4675C>T
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