Canonical Allele Identifier: CA778454242

Gene:

Linked Data

• dbSNP Id: rs1381742360
• MyVariant Identifiers: chr18:g.29336732C>T (hg19) ; chr18:g.31756769C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31756769C>T , CM000680.2:g.31756769C>T	GRCh38
NC_000018.9:g.29336732C>T , CM000680.1:g.29336732C>T	GRCh37
NC_000018.8:g.27590730C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935338.1:n.66-5370C>T