Canonical Allele Identifier: CA663648621

Gene:

Linked Data

• dbSNP Id: rs1427284241
• gnomAD v3: 10-30201899-T-C
• gnomAD v4: 10-30201899-T-C
• MyVariant Identifiers: chr10:g.30490828T>C (hg19) ; chr10:g.30201899T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.30201899T>C , CM000672.2:g.30201899T>C	GRCh38
NC_000010.10:g.30490828T>C , CM000672.1:g.30490828T>C	GRCh37
NC_000010.9:g.30530834T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_930791.1:n.1193-1588T>C
XR_930791.2:n.1449-1588T>C