ClinGen Allele Registry
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Canonical Allele Identifier:
CA632897701
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.39252576G>A
GRCh37
chr19:g.39743216G>A
Linked Data - Sequence & Population
gnomAD v2:
19:39743216 G / A
gnomAD v3:
19:39252576 G / A
gnomAD v4:
chr19-39252576-G-A
Linked Data - NCBI & NCI
dbSNP:
1274021688
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39252576G>A , CM000681.2:g.39252576G>A
GRCh38
NC_000019.9:g.39743216G>A , CM000681.1:g.39743216G>A
GRCh37
NC_000019.8:g.44435056G>A
NCBI36
NG_055295.1:g.1281C>T
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