Canonical Allele Identifier: CA665341640

Gene:

Linked Data

• dbSNP Id: rs1343569940
• gnomAD v3: 10-43318546-C-T
• gnomAD v4: 10-43318546-C-T
• MyVariant Identifiers: chr10:g.43813994C>T (hg19) ; chr10:g.43318546C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43318546C>T , CM000672.2:g.43318546C>T	GRCh38
NC_000010.10:g.43813994C>T , CM000672.1:g.43813994C>T	GRCh37
NC_000010.9:g.43134000C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945902.1:n.59C>T
XR_945902.2:n.149C>T