Canonical Allele Identifier: CA14667976

Gene:

Linked Data

• ClinVar Variation Id: 1261068
• ClinVar RCV Id: RCV001671469
• dbSNP Id: rs2075710
• gnomAD v2: 19-1106845-C-T
• gnomAD v3: 19-1106846-C-T
• gnomAD v4: 19-1106846-C-T
• MyVariant Identifiers: chr19:g.1106845C>T (hg19) ; chr19:g.1106846C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106846C>T , CM000681.2:g.1106846C>T	GRCh38
NC_000019.9:g.1106845C>T , CM000681.1:g.1106845C>T	GRCh37
NC_000019.8:g.1057845C>T	NCBI36
NG_050621.1:g.7921C>T