Canonical Allele Identifier: CA13443701

Gene:

Linked Data

• ClinVar Variation Id: 1237952
• ClinVar RCV Id: RCV001637500
• dbSNP Id: rs17593068
• gnomAD v2: 11-67350932-G-T
• gnomAD v3: 11-67583461-G-T
• gnomAD v4: 11-67583461-G-T
• MyVariant Identifiers: chr11:g.67350932G>T (hg19) ; chr11:g.67583461G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67583461G>T , CM000673.2:g.67583461G>T	GRCh38
NC_000011.9:g.67350932G>T , CM000673.1:g.67350932G>T	GRCh37
NC_000011.8:g.67107508G>T	NCBI36
NG_012075.1:g.4867G>T , LRG_723:g.4867G>T