Canonical Allele Identifier: CA14423808
Gene:
ClinVar RCV:
RCV001708050
ClinVar Variation:
1285756
dbSNP:
4292
gnomAD v2:
17:61554341 C / T
gnomAD v3:
17:63476980 C / T
gnomAD v4:
chr17-63476980-C-T
Joint Max Group AF 0.87906383 (AFR)
Genomes Max Group AF 0.87428457 (AFR)
Exomes Max Group AF 0.88174025 (AFR)
MyVariant.info:
GRCh38 chr17:g.63476980C>T
GRCh37 chr17:g.61554341C>T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63476980C>T , CM000679.2:g.63476980C>T GRCh38
NC_000017.10:g.61554341C>T , CM000679.1:g.61554341C>T GRCh37
NC_000017.9:g.58908073C>T NCBI36
NG_011648.1:g.4908C>T
Search 100 bp 5'
Search 100 bp 3'