Canonical Allele Identifier: CA14680564

Gene:

Linked Data

• ClinVar Variation Id: 1250296
• ClinVar RCV Id: RCV001652546
• dbSNP Id: rs17554931
• gnomAD v2: 19-1103785-C-T
• gnomAD v3: 19-1103786-C-T
• gnomAD v4: 19-1103786-C-T
• MyVariant Identifiers: chr19:g.1103785C>T (hg19) ; chr19:g.1103786C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1103786C>T , CM000681.2:g.1103786C>T	GRCh38
NC_000019.9:g.1103785C>T , CM000681.1:g.1103785C>T	GRCh37
NC_000019.8:g.1054785C>T	NCBI36
NG_050621.1:g.4861C>T