Canonical Allele Identifier: CA105563462

Gene:

Linked Data

• dbSNP Id: rs1001330378
• gnomAD v2: 4-126996399-C-T
• gnomAD v3: 4-126075244-C-T
• gnomAD v4: 4-126075244-C-T
• MyVariant Identifiers: chr4:g.126996399C>T (hg19) ; chr4:g.126075244C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.126075244C>T , CM000666.2:g.126075244C>T	GRCh38
NC_000004.11:g.126996399C>T , CM000666.1:g.126996399C>T	GRCh37
NC_000004.10:g.127215849C>T	NCBI36