ClinGen Allele Registry
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Canonical Allele Identifier:
CA15422411
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.68627895A>G
GRCh37
chr6:g.69337787A>G
Linked Data - Sequence & Population
gnomAD v2:
6:69337787 A / G
gnomAD v3:
6:68627895 A / G
gnomAD v4:
chr6-68627895-A-G
Joint Max Group AF
0.97684661 (EAS)
Genomes Max Group AF
0.97684661 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2585617
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.68627895A>G , CM000668.2:g.68627895A>G
GRCh38
NC_000006.11:g.69337787A>G , CM000668.1:g.69337787A>G
GRCh37
NC_000006.10:g.69394508A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_942664.1:n.1978T>C
Search 100 bp 5'
Search 100 bp 3'