Canonical Allele Identifier: CA2427731356
Gene: RP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46853541G= , CM000685.2:g.46853541G= GRCh38
NC_000023.10:g.46712976G= , CM000685.1:g.46712976G= GRCh37
NC_000023.9:g.46597920G= NCBI36
NG_009107.1:g.21630G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218340.4:c.168G= MANE Select ENSP00000218340.3:p.Thr56=
ENST00000218340.3:c.168G= ENSP00000218340.3:p.Thr56=
NM_006915.2:c.168G= NP_008846.2:p.Thr56=
NM_006915.3:c.168G= MANE Select NP_008846.2:p.Thr56=