ClinGen Allele Registry
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Canonical Allele Identifier:
CA308192762
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.39252476T>C
GRCh37
chr19:g.39743116T>C
Linked Data - Sequence & Population
gnomAD v3:
19:39252476 T / C
gnomAD v4:
chr19-39252476-T-C
Linked Data - NCBI & NCI
dbSNP:
565524963
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39252476T>C , CM000681.2:g.39252476T>C
GRCh38
NC_000019.9:g.39743116T>C , CM000681.1:g.39743116T>C
GRCh37
NC_000019.8:g.44434956T>C
NCBI36
NG_055295.1:g.1381A>G
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