Canonical Allele Identifier: CA13334210

Gene:

Linked Data

• ClinVar Variation Id: 1191355
• ClinVar RCV Id: RCV001552397
• dbSNP Id: rs17115144
• gnomAD v2: 10-104597308-G-A
• gnomAD v3: 10-102837551-G-A
• gnomAD v4: 10-102837551-G-A
• MyVariant Identifiers: chr10:g.104597308G>A (hg19) ; chr10:g.102837551G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102837551G>A , CM000672.2:g.102837551G>A	GRCh38
NC_000010.10:g.104597308G>A , CM000672.1:g.104597308G>A	GRCh37
NC_000010.9:g.104587298G>A	NCBI36
NG_007955.1:g.4983C>T