Canonical Allele Identifier: CA665341639

Gene:

Linked Data

• dbSNP Id: rs749389867
• gnomAD v3: 10-43318541-C-G
• gnomAD v4: 10-43318541-C-G
• MyVariant Identifiers: chr10:g.43813989C>G (hg19) ; chr10:g.43318541C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43318541C>G , CM000672.2:g.43318541C>G	GRCh38
NC_000010.10:g.43813989C>G , CM000672.1:g.43813989C>G	GRCh37
NC_000010.9:g.43133995C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945902.1:n.54C>G
XR_945902.2:n.144C>G