Canonical Allele Identifier: CA2665493181

Gene: NBEAL2

Linked Data

• gnomAD v4: 3-46999811-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46999811C>G , CM000665.2:g.46999811C>G	GRCh38
NC_000003.11:g.47041301C>G , CM000665.1:g.47041301C>G	GRCh37
NC_000003.10:g.47016305C>G	NCBI36
NG_031914.1:g.25129C>G , LRG_568:g.25129C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450053.8:c.3790-78C>G MANE Select	ENSP00000415034.2:n.3790-78C>G
ENST00000651747.1:c.3688-78C>G	ENSP00000499216.1:n.3688-78C>G
ENST00000652744.1:n.127-78C>G
ENST00000416683.5:c.1959+337C>G
ENST00000450053.7:c.3790-78C>G	ENSP00000415034.2:n.3790-78C>G
NM_015175.2:c.3790-78C>G , LRG_568t1:c.3790-78C>G	NP_055990.1:n.3790-78C>G
XM_005264992.2:c.3688-78C>G	XP_005265049.1:n.3688-78C>G
XM_005264993.2:c.262-78C>G	XP_005265050.1:n.262-78C>G
XM_006713072.2:c.3709-78C>G	XP_006713135.1:n.3709-78C>G
XM_011533532.1:c.3769-78C>G	XP_011531834.1:n.3769-78C>G
XM_011533533.1:c.3790-78C>G	XP_011531835.1:n.3790-78C>G
XM_011533534.1:c.3421-78C>G	XP_011531836.1:n.3421-78C>G
XM_011533535.1:c.3250-78C>G	XP_011531837.1:n.3250-78C>G
XM_011533536.1:c.3136-78C>G	XP_011531838.1:n.3136-78C>G
XM_011533537.1:c.2698-78C>G	XP_011531839.1:n.2698-78C>G
XR_940397.1:n.3966-78C>G
XR_940398.1:n.3966-78C>G
NM_001365116.1:c.3688-78C>G	NP_001352045.1:n.3688-78C>G
XM_006713072.3:c.3709-78C>G	XP_006713135.1:n.3709-78C>G
XM_011533533.2:c.3790-78C>G	XP_011531835.1:n.3790-78C>G
XM_017006010.1:c.3790-78C>G	XP_016861499.1:n.3790-78C>G
XM_017006011.1:c.3769-78C>G	XP_016861500.1:n.3769-78C>G
XM_017006012.1:c.3709-78C>G	XP_016861501.1:n.3709-78C>G
XM_017006013.1:c.3790-78C>G	XP_016861502.1:n.3790-78C>G
XM_017006014.1:c.3688-78C>G	XP_016861503.1:n.3688-78C>G
XM_017006015.1:c.3421-78C>G	XP_016861504.1:n.3421-78C>G
XM_017006016.1:c.3250-78C>G	XP_016861505.1:n.3250-78C>G
XM_017006017.1:c.262-78C>G	XP_016861506.1:n.262-78C>G
XR_940397.2:n.3966-78C>G
NM_001365116.2:c.3688-78C>G	NP_001352045.1:n.3688-78C>G
NM_015175.3:c.3790-78C>G MANE Select	NP_055990.1:n.3790-78C>G