Canonical Allele Identifier: CA299344136

Gene:

Linked Data

• dbSNP Id: rs746966845
• MyVariant Identifiers: chr18:g.39057739A>C (hg19) ; chr18:g.41477775A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.41477775A>C , CM000680.2:g.41477775A>C	GRCh38
NC_000018.9:g.39057739A>C , CM000680.1:g.39057739A>C	GRCh37
NC_000018.8:g.37311737A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_935409.1:n.86-26359A>C