Canonical Allele Identifier: CA1969379750
Gene: RAPSN HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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