Canonical Allele Identifier: CA659015384

Gene:

Linked Data

• dbSNP Id: rs1338810468
• gnomAD v3: 10-101750688-T-A
• gnomAD v4: 10-101750688-T-A
• MyVariant Identifiers: chr10:g.103510445T>A (hg19) ; chr10:g.101750688T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101750688T>A , CM000672.2:g.101750688T>A	GRCh38
NC_000010.10:g.103510445T>A , CM000672.1:g.103510445T>A	GRCh37
NC_000010.9:g.103500435T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_946255.1:n.217-6471A>T
XR_946255.2:n.217-6471A>T