Canonical Allele Identifier: CA202788787

Gene:

Linked Data

• dbSNP Id: rs1047835162
• gnomAD v2: 10-8739549-C-T
• gnomAD v3: 10-8697586-C-T
• gnomAD v4: 10-8697586-C-T
• MyVariant Identifiers: chr10:g.8739549C>T (hg19) ; chr10:g.8697586C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8697586C>T , CM000672.2:g.8697586C>T	GRCh38
NC_000010.10:g.8739549C>T , CM000672.1:g.8739549C>T	GRCh37
NC_000010.9:g.8779555C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930641.1:n.33-27785G>A