Canonical Allele Identifier: CA2427731355
Gene: RP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46853540C= , CM000685.2:g.46853540C= GRCh38
NC_000023.10:g.46712975C= , CM000685.1:g.46712975C= GRCh37
NC_000023.9:g.46597919C= NCBI36
NG_009107.1:g.21629C=

Transcript Alleles

HGVS Amino-acid change
ENST00000218340.4:c.167C= MANE Select ENSP00000218340.3:p.Thr56=
ENST00000218340.3:c.167C= ENSP00000218340.3:p.Thr56=
NM_006915.2:c.167C= NP_008846.2:p.Thr56=
NM_006915.3:c.167C= MANE Select NP_008846.2:p.Thr56=