Canonical Allele Identifier: CA778454180

Gene:

Linked Data

• dbSNP Id: rs1480691763
• MyVariant Identifiers: chr18:g.29336504A>G (hg19) ; chr18:g.31756541A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31756541A>G , CM000680.2:g.31756541A>G	GRCh38
NC_000018.9:g.29336504A>G , CM000680.1:g.29336504A>G	GRCh37
NC_000018.8:g.27590502A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935338.1:n.66-5598A>G