Canonical Allele Identifier: CA2332535310
Gene: RHPN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33041328C= , CM000681.2:g.33041328C= GRCh38
NC_000019.9:g.33532234C= , CM000681.1:g.33532234C= GRCh37
NC_000019.8:g.38224074C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000254260.8:c.185+2921G= MANE Select ENSP00000254260.2:n.185+2921G=
ENST00000254260.7:c.185+2921G= ENSP00000254260.2:n.185+2921G=
ENST00000588388.5:c.185+2921G= ENSP00000465898.1:n.185+2921G=
NM_033103.4:c.185+2921G= NP_149094.3:n.185+2921G=
NM_033103.5:c.185+2921G= MANE Select NP_149094.3:n.185+2921G=