Canonical Allele Identifier: CA206723613

Gene:

Linked Data

• dbSNP Id: rs558464716
• gnomAD v3: 10-43318556-C-T
• gnomAD v4: 10-43318556-C-T
• COSMIC: COSN26317636
• MyVariant Identifiers: chr10:g.43814004C>T (hg19) ; chr10:g.43318556C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43318556C>T , CM000672.2:g.43318556C>T	GRCh38
NC_000010.10:g.43814004C>T , CM000672.1:g.43814004C>T	GRCh37
NC_000010.9:g.43134010C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945902.1:n.69C>T
XR_945902.2:n.159C>T