Canonical Allele Identifier: CA110025488

Gene:

Linked Data

• dbSNP Id: rs1036828632
• gnomAD v2: 4-164012709-C-T
• gnomAD v3: 4-163091557-C-T
• gnomAD v4: 4-163091557-C-T
• MyVariant Identifiers: chr4:g.164012709C>T (hg19) ; chr4:g.163091557C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.163091557C>T , CM000666.2:g.163091557C>T	GRCh38
NC_000004.11:g.164012709C>T , CM000666.1:g.164012709C>T	GRCh37
NC_000004.10:g.164232159C>T	NCBI36