Canonical Allele Identifier: CA8197166

Gene:

Linked Data

• ClinVar Variation Id: 381203
• ClinVar RCV Id: RCV001720088
• dbSNP Id: rs557204298
• ExAC: 16:83932717 G / C
• gnomAD v2: 16-83932717-G-C
• gnomAD v3: 16-83899112-G-C
• gnomAD v4: 16-83899112-G-C
• MyVariant Identifiers: chr16:g.83932717G>C (hg19) ; chr16:g.83899112G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83899112G>C , CM000678.2:g.83899112G>C	GRCh38
NC_000016.9:g.83932717G>C , CM000678.1:g.83932717G>C	GRCh37
NC_000016.8:g.82490218G>C	NCBI36
NG_009079.1:g.4988G>C