Canonical Allele Identifier: CA202788792

Gene:

Linked Data

• dbSNP Id: rs150725833
• gnomAD v3: 10-8697632-G-T
• gnomAD v4: 10-8697632-G-T
• MyVariant Identifiers: chr10:g.8739595G>T (hg19) ; chr10:g.8697632G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8697632G>T , CM000672.2:g.8697632G>T	GRCh38
NC_000010.10:g.8739595G>T , CM000672.1:g.8739595G>T	GRCh37
NC_000010.9:g.8779601G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930641.1:n.33-27831C>A