Canonical Allele Identifier: CA413039473
Gene: RP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46853744A>T , CM000685.2:g.46853744A>T GRCh38
NC_000023.10:g.46713179A>T , CM000685.1:g.46713179A>T GRCh37
NC_000023.9:g.46598123A>T NCBI36
NG_009107.1:g.21833A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000218340.4:c.371A>T MANE Select ENSP00000218340.3:p.Lys124Met
ENST00000218340.3:c.371A>T ENSP00000218340.3:p.Lys124Met
NM_006915.2:c.371A>T NP_008846.2:p.Lys124Met
NM_006915.3:c.371A>T MANE Select NP_008846.2:p.Lys124Met