Canonical Allele Identifier: CA205533611

Gene:

Linked Data

• dbSNP Id: rs775725466
• gnomAD v3: 10-30201871-C-A
• gnomAD v4: 10-30201871-C-A
• MyVariant Identifiers: chr10:g.30490800C>A (hg19) ; chr10:g.30201871C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.30201871C>A , CM000672.2:g.30201871C>A	GRCh38
NC_000010.10:g.30490800C>A , CM000672.1:g.30490800C>A	GRCh37
NC_000010.9:g.30530806C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_930791.1:n.1193-1616C>A
XR_930791.2:n.1449-1616C>A