ClinGen Allele Registry
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Canonical Allele Identifier:
CA3713873
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.31575254G>A
GRCh37
chr6:g.31543031G>A
Linked Data - Sequence & Population
gnomAD v2:
6:31543031 G / A
gnomAD v3:
6:31575254 G / A
gnomAD v4:
chr6-31575254-G-A
Joint Max Group AF
0.16407824 (NFE)
Genomes Max Group AF
0.16815783 (NFE)
Exomes Max Group AF
0.16171478 (NFE)
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000211242
RCV001354056
RCV001807634
RCV001807635
RCV001807636
RCV001807637
RCV001807638
RCV001807639
RCV001807640
RCV001824024
RCV001836755
ClinVar Variation:
225964
dbSNP:
1800629
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.31575254G>A , CM000668.2:g.31575254G>A
GRCh38
NC_000006.11:g.31543031G>A , CM000668.1:g.31543031G>A
GRCh37
NC_000006.10:g.31651010G>A
NCBI36
NG_007462.1:g.4682G>A
NG_012010.1:g.8156G>A
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