Canonical Allele Identifier: CA522559873

Gene: EIF2B3

Linked Data

• ClinVar Variation Id: 2821284
• ClinVar RCV Id: RCV003711570
• dbSNP Id: rs549453394
• gnomAD v2: 1-45444139-G-A
• gnomAD v3: 1-44978467-G-A
• gnomAD v4: 1-44978467-G-A
• MyVariant Identifiers: chr1:g.45444139G>A (hg19) ; chr1:g.44978467G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.44978467G>A , CM000663.2:g.44978467G>A	GRCh38
NC_000001.10:g.45444139G>A , CM000663.1:g.45444139G>A	GRCh37
NC_000001.9:g.45216726G>A	NCBI36
NG_015864.1:g.13223C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360403.7:c.149-7C>T MANE Select	ENSP00000353575.2:n.149-7C>T
ENST00000360403.6:c.149-7C>T	ENSP00000353575.2:n.149-7C>T
ENST00000372182.6:n.262-7C>T
ENST00000372183.7:c.149-7C>T	ENSP00000361257.3:n.149-7C>T
ENST00000477953.5:n.252-7C>T
ENST00000480675.5:c.149-7C>T	ENSP00000485842.1:n.149-7C>T
ENST00000487532.5:n.261-7C>T
ENST00000497010.1:n.261-7C>T
ENST00000620860.4:c.149-7C>T	ENSP00000483996.1:n.149-7C>T
NM_001166588.2:c.149-7C>T	NP_001160060.1:n.149-7C>T
NM_001261418.1:c.149-7C>T	NP_001248347.1:n.149-7C>T
NM_020365.4:c.149-7C>T	NP_065098.1:n.149-7C>T
XM_011542396.1:c.149-7C>T	XP_011540698.1:n.149-7C>T
XM_017002745.2:c.149-7C>T	XP_016858234.1:n.149-7C>T
XM_017002746.1:c.-306-7C>T	XP_016858235.1:n.-306-7C>T
XM_017002747.1:c.-306-7C>T	XP_016858236.1:n.-306-7C>T
NM_020365.5:c.149-7C>T MANE Select	NP_065098.1:n.149-7C>T
NM_001166588.3:c.149-7C>T	NP_001160060.1:n.149-7C>T
NM_001261418.2:c.149-7C>T	NP_001248347.1:n.149-7C>T