Canonical Allele Identifier: CA10770925

Gene:

Linked Data

• ClinVar Variation Id: 1344496
• ClinVar RCV Id: RCV001848595
• dbSNP Id: rs11206510
• gnomAD v2: 1-55496039-T-C
• gnomAD v3: 1-55030366-T-C
• gnomAD v4: 1-55030366-T-C
• MyVariant Identifiers: chr1:g.55496039T>C (hg19) ; chr1:g.55030366T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55030366T>C , CM000663.2:g.55030366T>C	GRCh38
NC_000001.10:g.55496039T>C , CM000663.1:g.55496039T>C	GRCh37
NC_000001.9:g.55268627T>C	NCBI36