Linked Data
ClinVar Variation Id:
323298
dbSNP Id:
rs371656965
ExAC:
17:40695143 G / T
gnomAD v2:
17-40695143-G-T
gnomAD v3:
17-42543125-G-T
gnomAD v4:
17-42543125-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42543125G>T , CM000679.2:g.42543125G>T | GRCh38 |
| NC_000017.10:g.40695143G>T , CM000679.1:g.40695143G>T | GRCh37 |
| NC_000017.9:g.37948669G>T | NCBI36 |
| NG_011552.1:g.12193G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.1119G>T MANE Select | ENSP00000225927.1:p.Val373= | |
| ENST00000225927.6:c.1119G>T | ENSP00000225927.1:p.Val373= | |
| ENST00000591587.1:c.457G>T | ENSP00000467836.1:n.457G>T | |
| ENST00000592454.1:c.158G>T | ||
| NM_000263.3:c.1119G>T | NP_000254.2:p.Val373= | |
| XM_006721920.2:c.288G>T | XP_006721983.1:p.Val96= | |
| XM_011524840.1:c.120G>T | XP_011523142.1:p.Val40= | |
| XM_017024687.1:c.288G>T | XP_016880176.1:p.Val96= | |
| XM_024450771.1:c.1176G>T | XP_024306539.1:p.Val392= | |
| XM_024450772.1:c.120G>T | XP_024306540.1:p.Val40= | |
| NM_000263.4:c.1119G>T MANE Select | NP_000254.2:p.Val373= |