Linked Data
dbSNP Id:
rs1675657920
gnomAD v3:
2-37149158-T-C
gnomAD v4:
2-37149158-T-C
MyVariant Identifiers:
chr2:g.37376301T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.37149158T>C , CM000664.2:g.37149158T>C | GRCh38 |
| NC_000002.11:g.37376301T>C , CM000664.1:g.37376301T>C | GRCh37 |
| NC_000002.10:g.37229805T>C | NCBI36 |
| NG_030351.1:g.12890A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000233057.9:c.-183-135A>G (EIF2AK2) MANE Select | ENSP00000233057.4:n.-183-135A>G | |
| ENST00000411537.7:n.29-135A>G (EIF2AK2) | ||
| ENST00000679507.1:c.-16-1336A>G (EIF2AK2) | ENSP00000506024.1:n.-16-1336A>G | |
| ENST00000679979.1:c.-183-135A>G (EIF2AK2) | ENSP00000506455.1:n.-183-135A>G | |
| ENST00000680273.1:c.-183-135A>G (EIF2AK2) | ENSP00000506203.1:n.-183-135A>G | |
| ENST00000681329.1:n.157-135A>G (EIF2AK2) | ||
| ENST00000681463.1:c.-75-243A>G (EIF2AK2) | ENSP00000505138.1:n.-75-243A>G | |
| ENST00000681507.1:c.-99-219A>G (EIF2AK2) | ENSP00000505772.1:n.-99-219A>G | |
| ENST00000233057.8:c.-183-135A>G (EIF2AK2) | ENSP00000233057.4:n.-183-135A>G | |
| ENST00000390013.3:c.-99-219A>G (EIF2AK2) | ENSP00000374663.3:n.-99-219A>G | |
| ENST00000395127.6:c.-318A>G (EIF2AK2) | ENSP00000378559.2:n.-318A>G | |
| ENST00000411537.6:c.-75-243A>G (EIF2AK2) | ENSP00000393921.2:n.-75-243A>G | |
| ENST00000412776.1:n.629T>C (ARL14EPP1) | ||
| NM_001135651.2:c.-183-135A>G (EIF2AK2) | NP_001129123.1:n.-183-135A>G | |
| NM_002759.3:c.-318A>G (EIF2AK2) | NP_002750.1:n.-318A>G | |
| XM_011532987.1:c.-99-219A>G (EIF2AK2) | XP_011531289.1:n.-99-219A>G | |
| XM_011532987.2:c.-99-219A>G (EIF2AK2) | XP_011531289.1:n.-99-219A>G | |
| XM_017004503.1:c.-183-135A>G (EIF2AK2) | XP_016859992.1:n.-183-135A>G | |
| NM_001135651.3:c.-183-135A>G (EIF2AK2) MANE Select | NP_001129123.1:n.-183-135A>G | |
| NM_002759.4:c.-318A>G (EIF2AK2) | NP_002750.1:n.-318A>G |