Canonical Allele Identifier: CA4630573

Gene:

Linked Data

• ClinVar Variation Id: 910867
• ClinVar RCV Id: RCV001162991 ; RCV003945882
• dbSNP Id: rs767723868
• ExAC: 8:11422117 G / T
• gnomAD v2: 8-11422117-G-T
• gnomAD v3: 8-11564608-G-T
• gnomAD v4: 8-11564608-G-T
• MyVariant Identifiers: chr8:g.11422117G>T (hg19) ; chr8:g.11564608G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564608G>T , CM000670.2:g.11564608G>T	GRCh38
NC_000008.10:g.11422117G>T , CM000670.1:g.11422117G>T	GRCh37
NC_000008.9:g.11459526G>T	NCBI36
NG_023543.1:g.75597G>T
NG_023543.2:g.75597G>T