Canonical Allele Identifier: CA13931721

Gene:

Linked Data

• ClinVar Variation Id: 1297228
• ClinVar RCV Id: RCV001724932
• dbSNP Id: rs1003349
• gnomAD v2: 14-23305663-G-T
• gnomAD v3: 14-22836454-G-T
• gnomAD v4: 14-22836454-G-T
• MyVariant Identifiers: chr14:g.23305663G>T (hg19) ; chr14:g.22836454G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.22836454G>T , CM000676.2:g.22836454G>T	GRCh38
NC_000014.8:g.23305663G>T , CM000676.1:g.23305663G>T	GRCh37
NC_000014.7:g.22375503G>T	NCBI36
NG_046989.1:g.4922G>T