Canonical Allele Identifier: CA266827038

Gene:

Linked Data

• dbSNP Id: rs2956485
• gnomAD v3: 14-106768364-T-G
• gnomAD v4: 14-106768364-T-G
• MyVariant Identifiers: chr14:g.106768364T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.106768364T>G , CM000676.2:g.106768364T>G	GRCh38