ClinGen Allele Registry
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Canonical Allele Identifier:
CA13429178
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr11:g.113408708G>A
GRCh37
chr11:g.113279430G>A
Linked Data - Sequence & Population
gnomAD v2:
11:113279430 G / A
gnomAD v3:
11:113408708 G / A
gnomAD v4:
chr11-113408708-G-A
Joint Max Group AF
0.69385497 (NFE)
Genomes Max Group AF
0.69385497 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2242592
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.113408708G>A , CM000673.2:g.113408708G>A
GRCh38
NC_000011.9:g.113279430G>A , CM000673.1:g.113279430G>A
GRCh37
NC_000011.8:g.112784640G>A
NCBI36
NG_008841.1:g.71572C>T
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