Canonical Allele Identifier: CA2427731388
Gene: RP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46853667C= , CM000685.2:g.46853667C= GRCh38
NC_000023.10:g.46713102C= , CM000685.1:g.46713102C= GRCh37
NC_000023.9:g.46598046C= NCBI36
NG_009107.1:g.21756C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218340.4:c.294C= MANE Select ENSP00000218340.3:p.Gly98=
ENST00000218340.3:c.294C= ENSP00000218340.3:p.Gly98=
NM_006915.2:c.294C= NP_008846.2:p.Gly98=
NM_006915.3:c.294C= MANE Select NP_008846.2:p.Gly98=
Search 100 bp 5'
Search 100 bp 3'