Canonical Allele Identifier: CA433598404

Gene: NBEAL2

Linked Data

• dbSNP Id: rs2036861339
• MyVariant Identifiers: chr3:g.47041660C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47000170C>T , CM000665.2:g.47000170C>T	GRCh38
NC_000003.11:g.47041660C>T , CM000665.1:g.47041660C>T	GRCh37
NC_000003.10:g.47016664C>T	NCBI36
NG_031914.1:g.25488C>T , LRG_568:g.25488C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000450053.8:c.4071C>T MANE Select	ENSP00000415034.2:p.Asp1357=
ENST00000651747.1:c.3969C>T	ENSP00000499216.1:p.Asp1323=
ENST00000652744.1:n.408C>T
ENST00000416683.5:c.1960-26C>T
ENST00000450053.7:c.4071C>T	ENSP00000415034.2:p.Asp1357=
NM_015175.2:c.4071C>T , LRG_568t1:c.4071C>T	NP_055990.1:p.Asp1357=
XM_005264992.2:c.3969C>T	XP_005265049.1:p.Asp1323=
XM_005264993.2:c.543C>T	XP_005265050.1:p.Asp181=
XM_006713072.2:c.3990C>T	XP_006713135.1:p.Asp1330=
XM_011533532.1:c.4050C>T	XP_011531834.1:p.Asp1350=
XM_011533533.1:c.4071C>T	XP_011531835.1:p.Asp1357=
XM_011533534.1:c.3702C>T	XP_011531836.1:p.Asp1234=
XM_011533535.1:c.3531C>T	XP_011531837.1:p.Asp1177=
XM_011533536.1:c.3417C>T	XP_011531838.1:p.Asp1139=
XM_011533537.1:c.2979C>T	XP_011531839.1:p.Asp993=
XR_940397.1:n.4247C>T
XR_940398.1:n.4247C>T
NM_001365116.1:c.3969C>T	NP_001352045.1:p.Asp1323=
XM_006713072.3:c.3990C>T	XP_006713135.1:p.Asp1330=
XM_011533533.2:c.4071C>T	XP_011531835.1:p.Asp1357=
XM_017006010.1:c.4071C>T	XP_016861499.1:p.Asp1357=
XM_017006011.1:c.4050C>T	XP_016861500.1:p.Asp1350=
XM_017006012.1:c.3990C>T	XP_016861501.1:p.Asp1330=
XM_017006013.1:c.4071C>T	XP_016861502.1:p.Asp1357=
XM_017006014.1:c.3969C>T	XP_016861503.1:p.Asp1323=
XM_017006015.1:c.3702C>T	XP_016861504.1:p.Asp1234=
XM_017006016.1:c.3531C>T	XP_016861505.1:p.Asp1177=
XM_017006017.1:c.543C>T	XP_016861506.1:p.Asp181=
XR_940397.2:n.4247C>T
NM_001365116.2:c.3969C>T	NP_001352045.1:p.Asp1323=
NM_015175.3:c.4071C>T MANE Select	NP_055990.1:p.Asp1357=