Canonical Allele Identifier: CA776019716

Gene:

Linked Data

• dbSNP Id: rs1360380827
• MyVariant Identifiers: chr18:g.10321204G>A (hg19) ; chr18:g.10321207G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10321207G>A , CM000680.2:g.10321207G>A	GRCh38
NC_000018.9:g.10321204G>A , CM000680.1:g.10321204G>A	GRCh37
NC_000018.8:g.10311204G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935138.1:n.665+941C>T
XR_001753344.1:n.650+941C>T
XR_001753345.1:n.914C>T
XR_001753346.1:n.549+941C>T