Canonical Allele Identifier: CA433477140

Gene: NBEAL2

Linked Data

• MyVariant Identifiers: chr3:g.47041429A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46999939A>G , CM000665.2:g.46999939A>G	GRCh38
NC_000003.11:g.47041429A>G , CM000665.1:g.47041429A>G	GRCh37
NC_000003.10:g.47016433A>G	NCBI36
NG_031914.1:g.25257A>G , LRG_568:g.25257A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450053.8:c.3840A>G MANE Select	ENSP00000415034.2:p.Arg1280=
ENST00000651747.1:c.3738A>G	ENSP00000499216.1:p.Arg1246=
ENST00000652744.1:n.177A>G
ENST00000416683.5:c.1960-257A>G
ENST00000450053.7:c.3840A>G	ENSP00000415034.2:p.Arg1280=
NM_015175.2:c.3840A>G , LRG_568t1:c.3840A>G	NP_055990.1:p.Arg1280=
XM_005264992.2:c.3738A>G	XP_005265049.1:p.Arg1246=
XM_005264993.2:c.312A>G	XP_005265050.1:p.Arg104=
XM_006713072.2:c.3759A>G	XP_006713135.1:p.Arg1253=
XM_011533532.1:c.3819A>G	XP_011531834.1:p.Arg1273=
XM_011533533.1:c.3840A>G	XP_011531835.1:p.Arg1280=
XM_011533534.1:c.3471A>G	XP_011531836.1:p.Arg1157=
XM_011533535.1:c.3300A>G	XP_011531837.1:p.Arg1100=
XM_011533536.1:c.3186A>G	XP_011531838.1:p.Arg1062=
XM_011533537.1:c.2748A>G	XP_011531839.1:p.Arg916=
XR_940397.1:n.4016A>G
XR_940398.1:n.4016A>G
NM_001365116.1:c.3738A>G	NP_001352045.1:p.Arg1246=
XM_006713072.3:c.3759A>G	XP_006713135.1:p.Arg1253=
XM_011533533.2:c.3840A>G	XP_011531835.1:p.Arg1280=
XM_017006010.1:c.3840A>G	XP_016861499.1:p.Arg1280=
XM_017006011.1:c.3819A>G	XP_016861500.1:p.Arg1273=
XM_017006012.1:c.3759A>G	XP_016861501.1:p.Arg1253=
XM_017006013.1:c.3840A>G	XP_016861502.1:p.Arg1280=
XM_017006014.1:c.3738A>G	XP_016861503.1:p.Arg1246=
XM_017006015.1:c.3471A>G	XP_016861504.1:p.Arg1157=
XM_017006016.1:c.3300A>G	XP_016861505.1:p.Arg1100=
XM_017006017.1:c.312A>G	XP_016861506.1:p.Arg104=
XR_940397.2:n.4016A>G
NM_001365116.2:c.3738A>G	NP_001352045.1:p.Arg1246=
NM_015175.3:c.3840A>G MANE Select	NP_055990.1:p.Arg1280=