Canonical Allele Identifier: CA13240510

Gene:

Linked Data

• dbSNP Id: rs4747639
• gnomAD v2: 10-29364640-A-T
• gnomAD v3: 10-29075711-A-T
• gnomAD v4: 10-29075711-A-T
• MyVariant Identifiers: chr10:g.29364640A>T (hg19) ; chr10:g.29075711A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.29075711A>T , CM000672.2:g.29075711A>T	GRCh38
NC_000010.10:g.29364640A>T , CM000672.1:g.29364640A>T	GRCh37
NC_000010.9:g.29404646A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001747284.1:n.127-3781A>T