Canonical Allele Identifier: CA669472830

Gene:

Linked Data

• dbSNP Id: rs1425175139
• gnomAD v3: 10-8697453-G-C
• gnomAD v4: 10-8697453-G-C
• MyVariant Identifiers: chr10:g.8739416G>C (hg19) ; chr10:g.8697453G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8697453G>C , CM000672.2:g.8697453G>C	GRCh38
NC_000010.10:g.8739416G>C , CM000672.1:g.8739416G>C	GRCh37
NC_000010.9:g.8779422G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930641.1:n.33-27652C>G