Canonical Allele Identifier: CA2613410744
Gene: RAPSN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47449163G>T , CM000673.2:g.47449163G>T GRCh38
NC_000011.9:g.47470715G>T , CM000673.1:g.47470715G>T GRCh37
NC_000011.8:g.47427291G>T NCBI36
NG_008312.1:g.5016C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000298854.6:c.-199C>A ENSP00000298854.2:n.-199C>A
NM_005055.4:c.-199C>A NP_005046.2:n.-199C>A
NM_032645.4:c.-199C>A NP_116034.2:n.-199C>A