Canonical Allele Identifier: CA2200880116

Gene:

Linked Data

• ClinVar Variation Id: 1330145
• ClinVar RCV Id: RCV001801162
• dbSNP Id: rs1902034217
• gnomAD v4: 16-172837-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.172837G>A , CM000678.2:g.172837G>A	GRCh38
NC_000016.9:g.222836G>A , CM000678.1:g.222836G>A	GRCh37
NC_000016.8:g.162836G>A	NCBI36
NG_000006.1:g.33700G>A
NG_059186.1:g.1187G>A
NG_059271.1:g.4991G>A