Canonical Allele Identifier: CA11443646

Gene:

Linked Data

• dbSNP Id: rs4955935
• gnomAD v2: 3-55188514-C-T
• gnomAD v3: 3-55154487-C-T
• gnomAD v4: 3-55154487-C-T
• MyVariant Identifiers: chr3:g.55188514C>T (hg19) ; chr3:g.55154487C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.55154487C>T , CM000665.2:g.55154487C>T	GRCh38
NC_000003.11:g.55188514C>T , CM000665.1:g.55188514C>T	GRCh37
NC_000003.10:g.55163554C>T	NCBI36