ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA632897696
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.39252540A>G
GRCh37
chr19:g.39743180A>G
Linked Data - Sequence & Population
gnomAD v2:
19:39743180 A / G
gnomAD v3:
19:39252540 A / G
gnomAD v4:
chr19-39252540-A-G
Linked Data - NCBI & NCI
dbSNP:
1215251691
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39252540A>G , CM000681.2:g.39252540A>G
GRCh38
NC_000019.9:g.39743180A>G , CM000681.1:g.39743180A>G
GRCh37
NC_000019.8:g.44435020A>G
NCBI36
NG_055295.1:g.1317T>C
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