Canonical Allele Identifier: CA778454135

Gene:

Linked Data

• dbSNP Id: rs1253809692
• MyVariant Identifiers: chr18:g.29336400A>G (hg19) ; chr18:g.31756437A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31756437A>G , CM000680.2:g.31756437A>G	GRCh38
NC_000018.9:g.29336400A>G , CM000680.1:g.29336400A>G	GRCh37
NC_000018.8:g.27590398A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935338.1:n.66-5702A>G