Canonical Allele Identifier: CA202663805

Gene:

Linked Data

• dbSNP Id: rs1002283285
• MyVariant Identifiers: chr10:g.7089029G>A (hg19) ; chr10:g.7047067G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.7047067G>A , CM000672.2:g.7047067G>A	GRCh38
NC_000010.10:g.7089029G>A , CM000672.1:g.7089029G>A	GRCh37
NC_000010.9:g.7129035G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_930623.1:n.173-16750C>T
XR_930624.1:n.171-16750C>T
XR_930625.1:n.172-16750C>T
XR_930626.1:n.168-16750C>T
XR_930627.1:n.173-16750C>T
XR_001747351.1:n.364-16750C>T
XR_001747352.1:n.364-16750C>T
XR_001747353.1:n.188-34411C>T
XR_001747354.1:n.364-16750C>T
XR_930623.2:n.364-16750C>T
XR_930624.2:n.364-16750C>T
XR_930625.2:n.364-16750C>T
XR_930626.2:n.364-16750C>T
XR_930627.2:n.364-16750C>T