Canonical Allele Identifier: CA117794
Gene: RBBP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 5824
ClinVar RCV Id: RCV000006180
dbSNP Id: rs121434388

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.22992836A>G , CM000680.2:g.22992836A>G GRCh38
NC_000018.9:g.20572799A>G , CM000680.1:g.20572799A>G GRCh37
NC_000018.8:g.18826797A>G NCBI36
NG_012121.1:g.64505A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000327155.10:c.1009A>G MANE Select ENSP00000323050.5:p.Lys337Glu
ENST00000327155.9:c.1009A>G ENSP00000323050.5:p.Lys337Glu
ENST00000360790.9:c.1009A>G ENSP00000354024.5:p.Lys337Glu
ENST00000399721.6:c.1009A>G ENSP00000382627.2:p.Lys337Glu
ENST00000399722.6:c.1009A>G ENSP00000382628.2:p.Lys337Glu
ENST00000399725.6:c.1009A>G ENSP00000382630.2:p.Lys337Glu
NM_002894.2:c.1009A>G NP_002885.1:p.Lys337Glu
NM_203291.1:c.1009A>G NP_976036.1:p.Lys337Glu
NM_203292.1:c.1009A>G NP_976037.1:p.Lys337Glu
XM_005258325.1:c.1009A>G XP_005258382.1:p.Lys337Glu
XM_005258326.2:c.187A>G XP_005258383.1:p.Lys63Glu
XM_006722519.1:c.1009A>G XP_006722582.1:p.Lys337Glu
XM_006722520.1:c.1009A>G XP_006722583.1:p.Lys337Glu
XM_006722521.1:c.1009A>G XP_006722584.1:p.Lys337Glu
XM_011526132.1:c.1009A>G XP_011524434.1:p.Lys337Glu
XM_005258325.3:c.1009A>G XP_005258382.1:p.Lys337Glu
XM_005258326.4:c.187A>G XP_005258383.1:p.Lys63Glu
XM_006722519.2:c.1009A>G XP_006722582.1:p.Lys337Glu
XM_006722520.2:c.1009A>G XP_006722583.1:p.Lys337Glu
XM_006722521.2:c.1009A>G XP_006722584.1:p.Lys337Glu
XM_011526132.2:c.1009A>G XP_011524434.1:p.Lys337Glu
XM_017025916.1:c.187A>G XP_016881405.1:p.Lys63Glu
XM_024451233.1:c.715A>G XP_024307001.1:p.Lys239Glu
NM_002894.3:c.1009A>G MANE Select NP_002885.1:p.Lys337Glu
NM_203291.2:c.1009A>G NP_976036.1:p.Lys337Glu
NM_203292.2:c.1009A>G NP_976037.1:p.Lys337Glu