Canonical Allele Identifier: CA211819730

Gene: RPS3AP36

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95595157C>G , CM000672.2:g.95595157C>G	GRCh38
NC_000010.10:g.97354914C>G , CM000672.1:g.97354914C>G	GRCh37
NC_000010.9:g.97344904C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398190.2:n.560C>G