Linked Data
ClinVar Variation Id:
294687
dbSNP Id:
rs116246250
ExAC:
1:197404390 G / A
gnomAD v2:
1-197404390-G-A
gnomAD v3:
1-197435260-G-A
gnomAD v4:
1-197435260-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197435260G>A , CM000663.2:g.197435260G>A | GRCh38 |
| NC_000001.10:g.197404390G>A , CM000663.1:g.197404390G>A | GRCh37 |
| NC_000001.9:g.195671013G>A | NCBI36 |
| NG_008483.1:g.171983G>A | |
| NG_008483.2:g.238799G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367400.8:c.3397G>A MANE Select | ENSP00000356370.3:p.Val1133Met | |
| ENST00000638467.1:c.3397G>A | ENSP00000491102.1:p.Val1133Met | |
| ENST00000681519.1:c.2278G>A | ENSP00000505267.1:p.Val760Met | |
| ENST00000367397.1:c.1540G>A | ENSP00000356367.1:p.Val514Met | |
| ENST00000367399.6:c.3061G>A | ENSP00000356369.2:p.Val1021Met | |
| ENST00000367400.7:c.3397G>A | ENSP00000356370.3:p.Val1133Met | |
| ENST00000484075.5:c.3397G>A | ENSP00000433932.1:p.Val1133Met | |
| ENST00000535699.5:c.3325G>A | ENSP00000438786.1:p.Val1109Met | |
| ENST00000538660.5:c.2129-340G>A | ENSP00000438091.1:n.2129-340G>A | |
| NM_001193640.1:c.3061G>A | NP_001180569.1:p.Val1021Met | |
| NM_001257965.1:c.3325G>A | NP_001244894.1:p.Val1109Met | |
| NM_001257966.1:c.2129-340G>A | NP_001244895.1:n.2129-340G>A | |
| NM_201253.2:c.3397G>A | NP_957705.1:p.Val1133Met | |
| NR_047563.1:n.3398G>A | ||
| NR_047564.1:n.3606G>A | ||
| XM_011509365.1:c.3397G>A | XP_011507667.1:p.Val1133Met | |
| XM_011509366.1:c.3397G>A | XP_011507668.1:p.Val1133Met | |
| XM_011509367.1:c.3397G>A | XP_011507669.1:p.Val1133Met | |
| XM_011509368.1:c.2815G>A | XP_011507670.1:p.Val939Met | |
| XM_011509369.1:c.1840G>A | XP_011507671.1:p.Val614Met | |
| XM_011509365.2:c.3397G>A | XP_011507667.1:p.Val1133Met | |
| XM_011509369.2:c.1840G>A | XP_011507671.1:p.Val614Met | |
| XM_017000851.1:c.2554G>A | XP_016856340.1:p.Val852Met | |
| XM_017000852.1:c.3532G>A | XP_016856341.1:p.Val1178Met | |
| NM_201253.3:c.3397G>A MANE Select | NP_957705.1:p.Val1133Met | |
| NM_001193640.2:c.3061G>A | NP_001180569.1:p.Val1021Met | |
| NM_001257965.2:c.3325G>A | NP_001244894.1:p.Val1109Met | |
| NR_047563.2:n.3350G>A | ||
| NR_047564.2:n.3558G>A | ||
| NM_001257966.2:c.2129-340G>A | NP_001244895.1:n.2129-340G>A |