Canonical Allele Identifier: CA129689
Gene: NBEAL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 31119
ClinVar RCV Id: RCV000024115
dbSNP Id: rs387907114

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46995743A>T , CM000665.2:g.46995743A>T GRCh38
NC_000003.11:g.47037233A>T , CM000665.1:g.47037233A>T GRCh37
NC_000003.10:g.47012237A>T NCBI36
NG_031914.1:g.21061A>T , LRG_568:g.21061A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000450053.8:c.1928A>T MANE Select ENSP00000415034.2:p.Glu643Val
ENST00000651747.1:c.1826A>T ENSP00000499216.1:p.Glu609Val
ENST00000416683.5:c.343A>T
ENST00000450053.7:c.1928A>T ENSP00000415034.2:p.Glu643Val
NM_015175.2:c.1928A>T , LRG_568t1:c.1928A>T NP_055990.1:p.Glu643Val
XM_005264992.2:c.1826A>T XP_005265049.1:p.Glu609Val
XM_006713072.2:c.1847A>T XP_006713135.1:p.Glu616Val
XM_011533532.1:c.1907A>T XP_011531834.1:p.Glu636Val
XM_011533533.1:c.1928A>T XP_011531835.1:p.Glu643Val
XM_011533534.1:c.1559A>T XP_011531836.1:p.Glu520Val
XM_011533535.1:c.1388A>T XP_011531837.1:p.Glu463Val
XM_011533536.1:c.1274A>T XP_011531838.1:p.Glu425Val
XM_011533537.1:c.836A>T XP_011531839.1:p.Glu279Val
XR_940397.1:n.2104A>T
XR_940398.1:n.2104A>T
NM_001365116.1:c.1826A>T NP_001352045.1:p.Glu609Val
XM_006713072.3:c.1847A>T XP_006713135.1:p.Glu616Val
XM_011533533.2:c.1928A>T XP_011531835.1:p.Glu643Val
XM_017006010.1:c.1928A>T XP_016861499.1:p.Glu643Val
XM_017006011.1:c.1907A>T XP_016861500.1:p.Glu636Val
XM_017006012.1:c.1847A>T XP_016861501.1:p.Glu616Val
XM_017006013.1:c.1928A>T XP_016861502.1:p.Glu643Val
XM_017006014.1:c.1826A>T XP_016861503.1:p.Glu609Val
XM_017006015.1:c.1559A>T XP_016861504.1:p.Glu520Val
XM_017006016.1:c.1388A>T XP_016861505.1:p.Glu463Val
XR_940397.2:n.2104A>T
NM_001365116.2:c.1826A>T NP_001352045.1:p.Glu609Val
NM_015175.3:c.1928A>T MANE Select NP_055990.1:p.Glu643Val