Canonical Allele Identifier: CA174826672

Gene:

Linked Data

• ClinVar Variation Id: 1267861
• ClinVar RCV Id: RCV001678414
• dbSNP Id: rs8190878
• gnomAD v2: 8-30585670-G-C
• gnomAD v3: 8-30728153-G-C
• gnomAD v4: 8-30728153-G-C
• MyVariant Identifiers: chr8:g.30585670G>C (hg19) ; chr8:g.30728153G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.30728153G>C , CM000670.2:g.30728153G>C	GRCh38
NC_000008.10:g.30585670G>C , CM000670.1:g.30585670G>C	GRCh37
NC_000008.9:g.30705212G>C	NCBI36
NG_027719.1:g.4817C>G