Canonical Allele Identifier: CA1969379774
Community Standard Title: NC_000011.10:g.47449174T=
Gene: RAPSN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47449174T= , CM000673.2:g.47449174T= GRCh38
NC_000011.9:g.47470726T= , CM000673.1:g.47470726T= GRCh37
NC_000011.8:g.47427302T= NCBI36
NG_008312.1:g.5005A=

Transcript Alleles

HGVS Amino-acid Change
NM_005055.4:c.-210A= NP_005046.2:n.-210A=
NM_032645.4:c.-210A= NP_116034.2:n.-210A=
ENST00000298854.6:c.-210A= ENSP00000298854.2:n.-210A=