Canonical Allele Identifier: CA669450924

Gene:

Linked Data

• dbSNP Id: rs1349993415
• gnomAD v3: 10-8659190-A-G
• gnomAD v4: 10-8659190-A-G
• MyVariant Identifiers: chr10:g.8701153A>G (hg19) ; chr10:g.8659190A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8659190A>G , CM000672.2:g.8659190A>G	GRCh38
NC_000010.10:g.8701153A>G , CM000672.1:g.8701153A>G	GRCh37
NC_000010.9:g.8741159A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_930641.1:n.158T>C
XR_001747277.1:n.127T>C