Canonical Allele Identifier: CA776019151

Gene:

Linked Data

• dbSNP Id: rs1288561540
• MyVariant Identifiers: chr18:g.10382787G>T (hg19) ; chr18:g.10382790G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10382790G>T , CM000680.2:g.10382790G>T	GRCh38
NC_000018.9:g.10382787G>T , CM000680.1:g.10382787G>T	GRCh37
NC_000018.8:g.10372787G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_935143.1:n.919+1437G>T