Canonical Allele Identifier: CA433598255

Gene: NBEAL2

Linked Data

• dbSNP Id: rs2036866759
• MyVariant Identifiers: chr3:g.47041708T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47000218T>C , CM000665.2:g.47000218T>C	GRCh38
NC_000003.11:g.47041708T>C , CM000665.1:g.47041708T>C	GRCh37
NC_000003.10:g.47016712T>C	NCBI36
NG_031914.1:g.25536T>C , LRG_568:g.25536T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450053.8:c.4119T>C MANE Select	ENSP00000415034.2:p.Gly1373=
ENST00000651747.1:c.4017T>C	ENSP00000499216.1:p.Gly1339=
ENST00000652744.1:n.456T>C
ENST00000416683.5:c.1982T>C
ENST00000450053.7:c.4119T>C	ENSP00000415034.2:p.Gly1373=
NM_015175.2:c.4119T>C , LRG_568t1:c.4119T>C	NP_055990.1:p.Gly1373=
XM_005264992.2:c.4017T>C	XP_005265049.1:p.Gly1339=
XM_005264993.2:c.591T>C	XP_005265050.1:p.Gly197=
XM_006713072.2:c.4038T>C	XP_006713135.1:p.Gly1346=
XM_011533532.1:c.4098T>C	XP_011531834.1:p.Gly1366=
XM_011533533.1:c.4119T>C	XP_011531835.1:p.Gly1373=
XM_011533534.1:c.3750T>C	XP_011531836.1:p.Gly1250=
XM_011533535.1:c.3579T>C	XP_011531837.1:p.Gly1193=
XM_011533536.1:c.3465T>C	XP_011531838.1:p.Gly1155=
XM_011533537.1:c.3027T>C	XP_011531839.1:p.Gly1009=
XR_940397.1:n.4295T>C
XR_940398.1:n.4295T>C
NM_001365116.1:c.4017T>C	NP_001352045.1:p.Gly1339=
XM_006713072.3:c.4038T>C	XP_006713135.1:p.Gly1346=
XM_011533533.2:c.4119T>C	XP_011531835.1:p.Gly1373=
XM_017006010.1:c.4119T>C	XP_016861499.1:p.Gly1373=
XM_017006011.1:c.4098T>C	XP_016861500.1:p.Gly1366=
XM_017006012.1:c.4038T>C	XP_016861501.1:p.Gly1346=
XM_017006013.1:c.4119T>C	XP_016861502.1:p.Gly1373=
XM_017006014.1:c.4017T>C	XP_016861503.1:p.Gly1339=
XM_017006015.1:c.3750T>C	XP_016861504.1:p.Gly1250=
XM_017006016.1:c.3579T>C	XP_016861505.1:p.Gly1193=
XM_017006017.1:c.591T>C	XP_016861506.1:p.Gly197=
XR_940397.2:n.4295T>C
NM_001365116.2:c.4017T>C	NP_001352045.1:p.Gly1339=
NM_015175.3:c.4119T>C MANE Select	NP_055990.1:p.Gly1373=