ClinGen Allele Registry
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Canonical Allele Identifier:
CA72937008
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.38547672G>A
GRCh37
chr3:g.38589163G>A
Linked Data - Sequence & Population
gnomAD v2:
3:38589163 G / A
gnomAD v3:
3:38547672 G / A
gnomAD v4:
chr3-38547672-G-A
Joint Max Group AF
0.27683009 (MID)
Genomes Max Group AF
0.22892455 (NFE)
Linked Data - NCBI & NCI
dbSNP:
11129795
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.38547672G>A , CM000665.2:g.38547672G>A
GRCh38
NC_000003.11:g.38589163G>A , CM000665.1:g.38589163G>A
GRCh37
NC_000003.10:g.38564167G>A
NCBI36
NG_008934.1:g.107001C>T , LRG_289:g.107001C>T
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