Canonical Allele Identifier: CA10394188
Gene: RP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2797140
ClinVar RCV Id: RCV003671041
dbSNP Id: rs371935908
gnomAD v2: X-46712976-G-T
gnomAD v3: X-46853541-G-T
gnomAD v4: X-46853541-G-T

Genomic Alleles

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

Transcript Alleles

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