Canonical Allele Identifier: CA296576133

Gene:

Linked Data

• dbSNP Id: rs893814711
• MyVariant Identifiers: chr18:g.10382789T>G (hg19) ; chr18:g.10382792T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10382792T>G , CM000680.2:g.10382792T>G	GRCh38
NC_000018.9:g.10382789T>G , CM000680.1:g.10382789T>G	GRCh37
NC_000018.8:g.10372789T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_935143.1:n.919+1439T>G