Canonical Allele Identifier: CA2427731358
Gene: RP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46853550A= , CM000685.2:g.46853550A= GRCh38
NC_000023.10:g.46712985A= , CM000685.1:g.46712985A= GRCh37
NC_000023.9:g.46597929A= NCBI36
NG_009107.1:g.21639A=

Transcript Alleles

HGVS Amino-acid change
ENST00000218340.4:c.177A= MANE Select ENSP00000218340.3:p.Gly59=
ENST00000218340.3:c.177A= ENSP00000218340.3:p.Gly59=
NM_006915.2:c.177A= NP_008846.2:p.Gly59=
NM_006915.3:c.177A= MANE Select NP_008846.2:p.Gly59=