Canonical Allele Identifier: CA2332535378
Gene: RHPN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33041460C= , CM000681.2:g.33041460C= GRCh38
NC_000019.9:g.33532366C= , CM000681.1:g.33532366C= GRCh37
NC_000019.8:g.38224206C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000254260.8:c.185+2789G= MANE Select ENSP00000254260.2:n.185+2789G=
ENST00000254260.7:c.185+2789G= ENSP00000254260.2:n.185+2789G=
ENST00000588388.5:c.185+2789G= ENSP00000465898.1:n.185+2789G=
NM_033103.4:c.185+2789G= NP_149094.3:n.185+2789G=
NM_033103.5:c.185+2789G= MANE Select NP_149094.3:n.185+2789G=
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