Canonical Allele Identifier: CA14687734
Gene: RHPN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33036982T>C , CM000681.2:g.33036982T>C GRCh38
NC_000019.9:g.33527888T>C , CM000681.1:g.33527888T>C GRCh37
NC_000019.8:g.38219728T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000254260.8:c.185+7267A>G MANE Select ENSP00000254260.2:n.185+7267A>G
ENST00000254260.7:c.185+7267A>G ENSP00000254260.2:n.185+7267A>G
ENST00000588388.5:c.185+7267A>G ENSP00000465898.1:n.185+7267A>G
NM_033103.4:c.185+7267A>G NP_149094.3:n.185+7267A>G
NM_033103.5:c.185+7267A>G MANE Select NP_149094.3:n.185+7267A>G