Canonical Allele Identifier: CA2427731354
Gene: RP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46853536G= , CM000685.2:g.46853536G= GRCh38
NC_000023.10:g.46712971G= , CM000685.1:g.46712971G= GRCh37
NC_000023.9:g.46597915G= NCBI36
NG_009107.1:g.21625G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218340.4:c.163G= MANE Select ENSP00000218340.3:p.Gly55=
ENST00000218340.3:c.163G= ENSP00000218340.3:p.Gly55=
NM_006915.2:c.163G= NP_008846.2:p.Gly55=
NM_006915.3:c.163G= MANE Select NP_008846.2:p.Gly55=