ClinGen Allele Registry
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Canonical Allele Identifier:
CA177660170
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.55686989G>A
GRCh37
chr8:g.56599548G>A
Linked Data - Sequence & Population
gnomAD v2:
8:56599548 G / A
gnomAD v3:
8:55686989 G / A
gnomAD v4:
chr8-55686989-G-A
Joint Max Group AF
0.88689428 (AFR)
Genomes Max Group AF
0.88689428 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4737395
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.55686989G>A , CM000670.2:g.55686989G>A
GRCh38
NC_000008.10:g.56599548G>A , CM000670.1:g.56599548G>A
GRCh37
NC_000008.9:g.56762102G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'