Canonical Allele Identifier: CA10654593

Gene:

Linked Data

• ClinVar Variation Id: 369289
• ClinVar RCV Id: RCV000306442
• dbSNP Id: rs2547319
• gnomAD v2: 19-51883149-T-G
• gnomAD v3: 19-51379895-T-G
• gnomAD v4: 19-51379895-T-G
• MyVariant Identifiers: chr19:g.51883149T>G (hg19) ; chr19:g.51379895T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51379895T>G , CM000681.2:g.51379895T>G	GRCh38
NC_000019.9:g.51883149T>G , CM000681.1:g.51883149T>G	GRCh37
NC_000019.8:g.56574961T>G	NCBI36
NG_012924.1:g.13062A>C