Canonical Allele Identifier: CA10654587
Gene:

Linked Data

ClinVar Variation Id: 369261
ClinVar RCV Id: RCV000319369 RCV000376384
dbSNP Id: rs537572167
gnomAD v2: 19-18893570-C-G
gnomAD v3: 19-18782760-C-G
gnomAD v4: 19-18782760-C-G
MyVariant Identifiers: chr19:g.18893570C>G (hg19) chr19:g.18782760C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18782760C>G , CM000681.2:g.18782760C>G GRCh38
NC_000019.9:g.18893570C>G , CM000681.1:g.18893570C>G GRCh37
NC_000019.8:g.18754570C>G NCBI36
NG_007070.1:g.13545G>C
Search 100 bp 5'
Search 100 bp 3'