Canonical Allele Identifier: CA417472091

Gene: EIF2B3

Linked Data

• MyVariant Identifiers: chr1:g.45444122C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.44978450C>T , CM000663.2:g.44978450C>T	GRCh38
NC_000001.10:g.45444122C>T , CM000663.1:g.45444122C>T	GRCh37
NC_000001.9:g.45216709C>T	NCBI36
NG_015864.1:g.13240G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360403.7:c.159G>A MANE Select	ENSP00000353575.2:p.Val53=
ENST00000360403.6:c.159G>A	ENSP00000353575.2:p.Val53=
ENST00000372182.6:n.272G>A
ENST00000372183.7:c.159G>A	ENSP00000361257.3:p.Val53=
ENST00000477953.5:n.262G>A
ENST00000480675.5:c.159G>A	ENSP00000485842.1:p.Val53=
ENST00000487532.5:n.271G>A
ENST00000497010.1:n.271G>A
ENST00000620860.4:c.159G>A	ENSP00000483996.1:p.Val53=
NM_001166588.2:c.159G>A	NP_001160060.1:p.Val53=
NM_001261418.1:c.159G>A	NP_001248347.1:p.Val53=
NM_020365.4:c.159G>A	NP_065098.1:p.Val53=
XM_011542396.1:c.159G>A	XP_011540698.1:p.Val53=
XM_017002745.2:c.159G>A	XP_016858234.1:p.Val53=
XM_017002746.1:c.-296G>A	XP_016858235.1:n.-296G>A
XM_017002747.1:c.-296G>A	XP_016858236.1:n.-296G>A
NM_020365.5:c.159G>A MANE Select	NP_065098.1:p.Val53=
NM_001166588.3:c.159G>A	NP_001160060.1:p.Val53=
NM_001261418.2:c.159G>A	NP_001248347.1:p.Val53=