Canonical Allele Identifier: CA10654435

Gene:

Linked Data

• ClinVar Variation Id: 368864
• ClinVar RCV Id: RCV000275407 ; RCV000332869 ; RCV000389793 ; RCV001517584
• dbSNP Id: rs34743335
• gnomAD v2: 1-209979529-A-T
• gnomAD v3: 1-209806184-A-T
• gnomAD v4: 1-209806184-A-T
• MyVariant Identifiers: chr1:g.209979529A>T (hg19) ; chr1:g.209806184A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.209806184A>T , CM000663.2:g.209806184A>T	GRCh38
NC_000001.10:g.209979529A>T , CM000663.1:g.209979529A>T	GRCh37
NC_000001.9:g.208046152A>T	NCBI36
NG_007081.2:g.4951T>A