Canonical Allele Identifier: CA97479069

Gene:

Linked Data

• ClinVar Variation Id: 1196840
• ClinVar RCV Id: RCV001560464
• dbSNP Id: rs114379639
• gnomAD v2: 4-56212248-T-C
• gnomAD v3: 4-55346081-T-C
• gnomAD v4: 4-55346081-T-C
• MyVariant Identifiers: chr4:g.56212248T>C (hg19) ; chr4:g.55346081T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55346081T>C , CM000666.2:g.55346081T>C	GRCh38
NC_000004.11:g.56212248T>C , CM000666.1:g.56212248T>C	GRCh37
NC_000004.10:g.55907005T>C	NCBI36
NG_028230.1:g.4861T>C