Canonical Allele Identifier: CA666857958

Gene:

Linked Data

• dbSNP Id: rs1404703355
• MyVariant Identifiers: chr10:g.59572335T>A (hg19) ; chr10:g.57812575T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.57812575T>A , CM000672.2:g.57812575T>A	GRCh38
NC_000010.10:g.59572335T>A , CM000672.1:g.59572335T>A	GRCh37
NC_000010.9:g.59242341T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945979.1:n.68+34717A>T
XR_001747454.1:n.85+34717A>T