Canonical Allele Identifier: CA10587996
Gene: RAPSN HGNC NCBI

Linked Data

ClinVar Variation Id: 264677
dbSNP Id: rs886037842

Genomic Alleles

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

Transcript Alleles

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