Canonical Allele Identifier: CA744879952

Gene: RPS4XP2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.4675114C>G , CM000682.2:g.4675114C>G	GRCh38
NC_000020.10:g.4655760C>G , CM000682.1:g.4655760C>G	GRCh37
NC_000020.9:g.4603760C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652447.1:n.87+9948G>C