ClinGen Allele Registry
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Canonical Allele Identifier:
CA14642619
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.39241861T>C
GRCh37
chr19:g.39732501T>C
Linked Data - Sequence & Population
gnomAD v2:
19:39732501 T / C
gnomAD v3:
19:39241861 T / C
gnomAD v4:
chr19-39241861-T-C
Joint Max Group AF
0.26852749 (AMR)
Genomes Max Group AF
0.26852749 (AMR)
Linked Data - NCBI & NCI
dbSNP:
8105790
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39241861T>C , CM000681.2:g.39241861T>C
GRCh38
NC_000019.9:g.39732501T>C , CM000681.1:g.39732501T>C
GRCh37
NC_000019.8:g.44424341T>C
NCBI36
NG_042193.1:g.8111A>G
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