Canonical Allele Identifier: CA433477095

Gene: NBEAL2

Linked Data

• dbSNP Id: rs2107382401
• MyVariant Identifiers: chr3:g.47041390C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46999900C>A , CM000665.2:g.46999900C>A	GRCh38
NC_000003.11:g.47041390C>A , CM000665.1:g.47041390C>A	GRCh37
NC_000003.10:g.47016394C>A	NCBI36
NG_031914.1:g.25218C>A , LRG_568:g.25218C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450053.8:c.3801C>A MANE Select	ENSP00000415034.2:p.Leu1267=
ENST00000651747.1:c.3699C>A	ENSP00000499216.1:p.Leu1233=
ENST00000652744.1:n.138C>A
ENST00000416683.5:c.1960-296C>A
ENST00000450053.7:c.3801C>A	ENSP00000415034.2:p.Leu1267=
NM_015175.2:c.3801C>A , LRG_568t1:c.3801C>A	NP_055990.1:p.Leu1267=
XM_005264992.2:c.3699C>A	XP_005265049.1:p.Leu1233=
XM_005264993.2:c.273C>A	XP_005265050.1:p.Leu91=
XM_006713072.2:c.3720C>A	XP_006713135.1:p.Leu1240=
XM_011533532.1:c.3780C>A	XP_011531834.1:p.Leu1260=
XM_011533533.1:c.3801C>A	XP_011531835.1:p.Leu1267=
XM_011533534.1:c.3432C>A	XP_011531836.1:p.Leu1144=
XM_011533535.1:c.3261C>A	XP_011531837.1:p.Leu1087=
XM_011533536.1:c.3147C>A	XP_011531838.1:p.Leu1049=
XM_011533537.1:c.2709C>A	XP_011531839.1:p.Leu903=
XR_940397.1:n.3977C>A
XR_940398.1:n.3977C>A
NM_001365116.1:c.3699C>A	NP_001352045.1:p.Leu1233=
XM_006713072.3:c.3720C>A	XP_006713135.1:p.Leu1240=
XM_011533533.2:c.3801C>A	XP_011531835.1:p.Leu1267=
XM_017006010.1:c.3801C>A	XP_016861499.1:p.Leu1267=
XM_017006011.1:c.3780C>A	XP_016861500.1:p.Leu1260=
XM_017006012.1:c.3720C>A	XP_016861501.1:p.Leu1240=
XM_017006013.1:c.3801C>A	XP_016861502.1:p.Leu1267=
XM_017006014.1:c.3699C>A	XP_016861503.1:p.Leu1233=
XM_017006015.1:c.3432C>A	XP_016861504.1:p.Leu1144=
XM_017006016.1:c.3261C>A	XP_016861505.1:p.Leu1087=
XM_017006017.1:c.273C>A	XP_016861506.1:p.Leu91=
XR_940397.2:n.3977C>A
NM_001365116.2:c.3699C>A	NP_001352045.1:p.Leu1233=
NM_015175.3:c.3801C>A MANE Select	NP_055990.1:p.Leu1267=