Canonical Allele Identifier: CA206723612

Gene:

Linked Data

• dbSNP Id: rs539725093
• gnomAD v3: 10-43318547-C-T
• gnomAD v4: 10-43318547-C-T
• MyVariant Identifiers: chr10:g.43813995C>T (hg19) ; chr10:g.43318547C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43318547C>T , CM000672.2:g.43318547C>T	GRCh38
NC_000010.10:g.43813995C>T , CM000672.1:g.43813995C>T	GRCh37
NC_000010.9:g.43134001C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945902.1:n.60C>T
XR_945902.2:n.150C>T