Canonical Allele Identifier: CA267219911

Gene:

Linked Data

• dbSNP Id: rs911333702
• gnomAD v2: 14-104017969-C-T
• gnomAD v3: 14-103551632-C-T
• gnomAD v4: 14-103551632-C-T
• MyVariant Identifiers: chr14:g.104017969C>T (hg19) ; chr14:g.104017969_104017972delinsTGGT (hg19) ; chr14:g.103551632C>T (hg38) ; chr14:g.103551632_103551635delinsTGGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103551632C>T , CM000676.2:g.103551632C>T	GRCh38
NC_000014.8:g.104017969C>T , CM000676.1:g.104017969C>T	GRCh37
NC_000014.7:g.103087722C>T	NCBI36