Linked Data
ClinVar Variation Id:
522822
dbSNP Id:
rs555145190
gnomAD v4:
17-42543921-G-T
COSMIC:
COSM3970073
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42543921G>T , CM000679.2:g.42543921G>T | GRCh38 |
| NC_000017.10:g.40695939G>T , CM000679.1:g.40695939G>T | GRCh37 |
| NC_000017.9:g.37949465G>T | NCBI36 |
| NG_011552.1:g.12989G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.1915G>T MANE Select | ENSP00000225927.1:p.Glu639Ter | |
| ENST00000225927.6:c.1915G>T | ENSP00000225927.1:p.Glu639Ter | |
| ENST00000591587.1:c.1253G>T | ENSP00000467836.1:n.1253G>T | |
| NM_000263.3:c.1915G>T | NP_000254.2:p.Glu639Ter | |
| XM_006721920.2:c.1084G>T | XP_006721983.1:p.Glu362Ter | |
| XM_011524840.1:c.916G>T | XP_011523142.1:p.Glu306Ter | |
| XM_017024687.1:c.1084G>T | XP_016880176.1:p.Glu362Ter | |
| XM_024450771.1:c.1972G>T | XP_024306539.1:p.Glu658Ter | |
| XM_024450772.1:c.916G>T | XP_024306540.1:p.Glu306Ter | |
| NM_000263.4:c.1915G>T MANE Select | NP_000254.2:p.Glu639Ter |