Canonical Allele Identifier: CA212877316

Gene:

Linked Data

• dbSNP Id: rs1046652217
• MyVariant Identifiers: chr10:g.101861504T>A (hg19) ; chr10:g.100101747T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100101747T>A , CM000672.2:g.100101747T>A	GRCh38
NC_000010.10:g.101861504T>A , CM000672.1:g.101861504T>A	GRCh37
NC_000010.9:g.101851494T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_946245.1:n.185+5510T>A