Linked Data
dbSNP Id:
rs2110027525
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55110523C>T , CM000666.2:g.55110523C>T | GRCh38 |
| NC_000004.11:g.55976690C>T , CM000666.1:g.55976690C>T | GRCh37 |
| NC_000004.10:g.55671447C>T | NCBI36 |
| NG_012004.1:g.20073G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263923.5:c.1135G>A MANE Select | ENSP00000263923.4:p.Ala379Thr | |
| ENST00000647068.1:n.1148G>A | ||
| ENST00000263923.4:c.1135G>A | ENSP00000263923.4:p.Ala379Thr | |
| ENST00000512566.1:n.1135G>A | ||
| NM_002253.2:c.1135G>A | NP_002244.1:p.Ala379Thr | |
| NM_002253.3:c.1135G>A | NP_002244.1:p.Ala379Thr | |
| NM_002253.4:c.1135G>A MANE Select | NP_002244.1:p.Ala379Thr |