Linked Data
dbSNP Id:
rs2117622124
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.18400296T>C , CM000670.2:g.18400296T>C | GRCh38 |
| NC_000008.10:g.18257806T>C , CM000670.1:g.18257806T>C | GRCh37 |
| NC_000008.9:g.18302086T>C | NCBI36 |
| NG_012246.1:g.14052T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000286479.4:c.293T>C MANE Select | ENSP00000286479.3:p.Val98Ala | |
| ENST00000286479.3:c.293T>C | ENSP00000286479.3:p.Val98Ala | |
| ENST00000520116.1:c.-57-41T>C | ENSP00000428416.1:n.-57-41T>C | |
| NM_000015.2:c.293T>C | NP_000006.2:p.Val98Ala | |
| XM_011544358.1:c.293T>C | XP_011542660.1:p.Val98Ala | |
| XM_017012938.1:c.293T>C | XP_016868427.1:p.Val98Ala | |
| NM_000015.3:c.293T>C MANE Select | NP_000006.2:p.Val98Ala |