Canonical Allele Identifier: CA1268229047
Gene: EIF2AK3 HGNC NCBI

Linked Data

dbSNP Id: rs1675826554
gnomAD v3: 2-88625123-T-C
gnomAD v4: 2-88625123-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88625123T>C , CM000664.2:g.88625123T>C GRCh38
NC_000002.11:g.88924641T>C , CM000664.1:g.88924641T>C GRCh37
NC_000002.10:g.88705756T>C NCBI36
NG_016424.1:g.7454A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682892.1:c.-145-11270A>G ENSP00000507214.1:n.-145-11270A>G
ENST00000303236.9:c.308+1844A>G MANE Select ENSP00000307235.3:n.308+1844A>G
ENST00000652099.1:c.306+1844A>G
ENST00000652423.1:c.184+1844A>G ENSP00000498948.1:n.184+1844A>G
ENST00000303236.7:c.308+1844A>G ENSP00000307235.3:n.308+1844A>G
NM_004836.5:c.308+1844A>G NP_004827.4:n.308+1844A>G
NM_004836.6:c.308+1844A>G NP_004827.4:n.308+1844A>G
XR_939749.1:n.517+1844A>G
XM_017005376.2:c.-573+1844A>G XP_016860865.1:n.-573+1844A>G
NM_004836.7:c.308+1844A>G MANE Select NP_004827.4:n.308+1844A>G