Canonical Allele Identifier: CA112757665

Gene:

Linked Data

• dbSNP Id: rs980203276
• gnomAD v2: 4-189861535-A-T
• gnomAD v3: 4-188940381-A-T
• gnomAD v4: 4-188940381-A-T
• MyVariant Identifiers: chr4:g.189861535A>T (hg19) ; chr4:g.188940381A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.188940381A>T , CM000666.2:g.188940381A>T	GRCh38
NC_000004.11:g.189861535A>T , CM000666.1:g.189861535A>T	GRCh37
NC_000004.10:g.190098529A>T	NCBI36