Canonical Allele Identifier: CA73817487
Gene: NBEAL2 HGNC NCBI

Linked Data

dbSNP Id: rs779385923
gnomAD v2: 3-47041425-C-T
gnomAD v4: 3-46999935-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46999935C>T , CM000665.2:g.46999935C>T GRCh38
NC_000003.11:g.47041425C>T , CM000665.1:g.47041425C>T GRCh37
NC_000003.10:g.47016429C>T NCBI36
NG_031914.1:g.25253C>T , LRG_568:g.25253C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000450053.8:c.3836C>T MANE Select ENSP00000415034.2:p.Ala1279Val
ENST00000651747.1:c.3734C>T ENSP00000499216.1:p.Ala1245Val
ENST00000652744.1:n.173C>T
ENST00000416683.5:c.1960-261C>T
ENST00000450053.7:c.3836C>T ENSP00000415034.2:p.Ala1279Val
NM_015175.2:c.3836C>T , LRG_568t1:c.3836C>T NP_055990.1:p.Ala1279Val
XM_005264992.2:c.3734C>T XP_005265049.1:p.Ala1245Val
XM_005264993.2:c.308C>T XP_005265050.1:p.Ala103Val
XM_006713072.2:c.3755C>T XP_006713135.1:p.Ala1252Val
XM_011533532.1:c.3815C>T XP_011531834.1:p.Ala1272Val
XM_011533533.1:c.3836C>T XP_011531835.1:p.Ala1279Val
XM_011533534.1:c.3467C>T XP_011531836.1:p.Ala1156Val
XM_011533535.1:c.3296C>T XP_011531837.1:p.Ala1099Val
XM_011533536.1:c.3182C>T XP_011531838.1:p.Ala1061Val
XM_011533537.1:c.2744C>T XP_011531839.1:p.Ala915Val
XR_940397.1:n.4012C>T
XR_940398.1:n.4012C>T
NM_001365116.1:c.3734C>T NP_001352045.1:p.Ala1245Val
XM_006713072.3:c.3755C>T XP_006713135.1:p.Ala1252Val
XM_011533533.2:c.3836C>T XP_011531835.1:p.Ala1279Val
XM_017006010.1:c.3836C>T XP_016861499.1:p.Ala1279Val
XM_017006011.1:c.3815C>T XP_016861500.1:p.Ala1272Val
XM_017006012.1:c.3755C>T XP_016861501.1:p.Ala1252Val
XM_017006013.1:c.3836C>T XP_016861502.1:p.Ala1279Val
XM_017006014.1:c.3734C>T XP_016861503.1:p.Ala1245Val
XM_017006015.1:c.3467C>T XP_016861504.1:p.Ala1156Val
XM_017006016.1:c.3296C>T XP_016861505.1:p.Ala1099Val
XM_017006017.1:c.308C>T XP_016861506.1:p.Ala103Val
XR_940397.2:n.4012C>T
NM_001365116.2:c.3734C>T NP_001352045.1:p.Ala1245Val
NM_015175.3:c.3836C>T MANE Select NP_055990.1:p.Ala1279Val