ClinGen Allele Registry
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Canonical Allele Identifier:
CA14642776
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.39738769C>G
GRCh37
chr19:g.40229409C>G
Linked Data - Sequence & Population
gnomAD v2:
19:40229409 C / G
gnomAD v3:
19:39738769 C / G
gnomAD v4:
chr19-39738769-C-G
Joint Max Group AF
0.34241591 (NFE)
Genomes Max Group AF
0.34241591 (NFE)
Linked Data - NCBI & NCI
dbSNP:
12611334
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39738769C>G , CM000681.2:g.39738769C>G
GRCh38
NC_000019.9:g.40229409C>G , CM000681.1:g.40229409C>G
GRCh37
NC_000019.8:g.44921249C>G
NCBI36
NG_046978.1:g.4261G>C
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