Canonical Allele Identifier: CA2548563361
Gene: RHPN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33041346G>T , CM000681.2:g.33041346G>T GRCh38
NC_000019.9:g.33532252G>T , CM000681.1:g.33532252G>T GRCh37
NC_000019.8:g.38224092G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000254260.8:c.185+2903C>A MANE Select ENSP00000254260.2:n.185+2903C>A
ENST00000254260.7:c.185+2903C>A ENSP00000254260.2:n.185+2903C>A
ENST00000588388.5:c.185+2903C>A ENSP00000465898.1:n.185+2903C>A
NM_033103.4:c.185+2903C>A NP_149094.3:n.185+2903C>A
NM_033103.5:c.185+2903C>A MANE Select NP_149094.3:n.185+2903C>A
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