Canonical Allele Identifier: CA13272908
Gene: RPS3AP36 HGNC NCBI

Linked Data

dbSNP Id: rs498055

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000398190.2:n.560C>T