Linked Data
dbSNP Id:
rs1675655143
gnomAD v4:
2-37149084-G-A
MyVariant Identifiers:
chr2:g.37376227G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.37149084G>A , CM000664.2:g.37149084G>A | GRCh38 |
| NC_000002.11:g.37376227G>A , CM000664.1:g.37376227G>A | GRCh37 |
| NC_000002.10:g.37229731G>A | NCBI36 |
| NG_030351.1:g.12964C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233057.9:c.-183-61C>T (EIF2AK2) MANE Select | ENSP00000233057.4:n.-183-61C>T | |
| ENST00000411537.7:n.29-61C>T (EIF2AK2) | ||
| ENST00000679507.1:c.-16-1262C>T (EIF2AK2) | ENSP00000506024.1:n.-16-1262C>T | |
| ENST00000679979.1:c.-183-61C>T (EIF2AK2) | ENSP00000506455.1:n.-183-61C>T | |
| ENST00000680273.1:c.-183-61C>T (EIF2AK2) | ENSP00000506203.1:n.-183-61C>T | |
| ENST00000681329.1:n.157-61C>T (EIF2AK2) | ||
| ENST00000681463.1:c.-75-169C>T (EIF2AK2) | ENSP00000505138.1:n.-75-169C>T | |
| ENST00000681507.1:c.-99-145C>T (EIF2AK2) | ENSP00000505772.1:n.-99-145C>T | |
| ENST00000233057.8:c.-183-61C>T (EIF2AK2) | ENSP00000233057.4:n.-183-61C>T | |
| ENST00000390013.3:c.-99-145C>T (EIF2AK2) | ENSP00000374663.3:n.-99-145C>T | |
| ENST00000395127.6:c.-244C>T (EIF2AK2) | ENSP00000378559.2:n.-244C>T | |
| ENST00000411537.6:c.-75-169C>T (EIF2AK2) | ENSP00000393921.2:n.-75-169C>T | |
| ENST00000412776.1:n.555G>A (ARL14EPP1) | ||
| NM_001135651.2:c.-183-61C>T (EIF2AK2) | NP_001129123.1:n.-183-61C>T | |
| NM_002759.3:c.-244C>T (EIF2AK2) | NP_002750.1:n.-244C>T | |
| XM_011532987.1:c.-99-145C>T (EIF2AK2) | XP_011531289.1:n.-99-145C>T | |
| XM_011532987.2:c.-99-145C>T (EIF2AK2) | XP_011531289.1:n.-99-145C>T | |
| XM_017004503.1:c.-183-61C>T (EIF2AK2) | XP_016859992.1:n.-183-61C>T | |
| NM_001135651.3:c.-183-61C>T (EIF2AK2) MANE Select | NP_001129123.1:n.-183-61C>T | |
| NM_002759.4:c.-244C>T (EIF2AK2) | NP_002750.1:n.-244C>T |