Canonical Allele Identifier: CA13804849
Gene:

Linked Data

ClinVar Variation Id: 1235754
ClinVar RCV Id: RCV001619352
dbSNP Id: rs117685390
gnomAD v2: 13-20767309-A-G
gnomAD v3: 13-20193170-A-G
gnomAD v4: 13-20193170-A-G
MyVariant Identifiers: chr13:g.20767309A>G (hg19) chr13:g.20193170A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20193170A>G , CM000675.2:g.20193170A>G GRCh38
NC_000013.10:g.20767309A>G , CM000675.1:g.20767309A>G GRCh37
NC_000013.9:g.19665309A>G NCBI36
NG_008358.1:g.4806T>C
Search 100 bp 5'
Search 100 bp 3'