Canonical Allele Identifier: CA202825344

Gene:

Linked Data

• dbSNP Id: rs930440205
• gnomAD v3: 10-9011177-G-T
• gnomAD v4: 10-9011177-G-T
• MyVariant Identifiers: chr10:g.9053140G>T (hg19) ; chr10:g.9011177G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.9011177G>T , CM000672.2:g.9011177G>T	GRCh38
NC_000010.10:g.9053140G>T , CM000672.1:g.9053140G>T	GRCh37
NC_000010.9:g.9093146G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_930641.1:n.32+54186C>A