Linked Data
ClinVar Variation Id:
294681
dbSNP Id:
rs534108312
ExAC:
1:197398617 G / A
gnomAD v2:
1-197398617-G-A
gnomAD v3:
1-197429487-G-A
gnomAD v4:
1-197429487-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197429487G>A , CM000663.2:g.197429487G>A | GRCh38 |
| NC_000001.10:g.197398617G>A , CM000663.1:g.197398617G>A | GRCh37 |
| NC_000001.9:g.195665240G>A | NCBI36 |
| NG_008483.1:g.166210G>A | |
| NG_008483.2:g.233026G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367400.8:c.2715G>A MANE Select | ENSP00000356370.3:p.Arg905= | |
| ENST00000638467.1:c.2715G>A | ENSP00000491102.1:p.Arg905= | |
| ENST00000681519.1:c.1596G>A | ENSP00000505267.1:p.Arg532= | |
| ENST00000367397.1:c.858G>A | ENSP00000356367.1:p.Arg286= | |
| ENST00000367399.6:c.2379G>A | ENSP00000356369.2:p.Arg793= | |
| ENST00000367400.7:c.2715G>A | ENSP00000356370.3:p.Arg905= | |
| ENST00000484075.5:c.2715G>A | ENSP00000433932.1:p.Arg905= | |
| ENST00000535699.5:c.2643G>A | ENSP00000438786.1:p.Arg881= | |
| ENST00000538660.5:c.2129-6113G>A | ENSP00000438091.1:n.2129-6113G>A | |
| NM_001193640.1:c.2379G>A | NP_001180569.1:p.Arg793= | |
| NM_001257965.1:c.2643G>A | NP_001244894.1:p.Arg881= | |
| NM_001257966.1:c.2129-6113G>A | NP_001244895.1:n.2129-6113G>A | |
| NM_201253.2:c.2715G>A | NP_957705.1:p.Arg905= | |
| NR_047563.1:n.2716G>A | ||
| NR_047564.1:n.2924G>A | ||
| XM_011509365.1:c.2715G>A | XP_011507667.1:p.Arg905= | |
| XM_011509366.1:c.2715G>A | XP_011507668.1:p.Arg905= | |
| XM_011509367.1:c.2715G>A | XP_011507669.1:p.Arg905= | |
| XM_011509368.1:c.2133G>A | XP_011507670.1:p.Arg711= | |
| XM_011509369.1:c.1158G>A | XP_011507671.1:p.Arg386= | |
| XM_011509365.2:c.2715G>A | XP_011507667.1:p.Arg905= | |
| XM_011509369.2:c.1158G>A | XP_011507671.1:p.Arg386= | |
| XM_017000851.1:c.1872G>A | XP_016856340.1:p.Arg624= | |
| XM_017000852.1:c.2850G>A | XP_016856341.1:p.Arg950= | |
| NM_201253.3:c.2715G>A MANE Select | NP_957705.1:p.Arg905= | |
| NM_001193640.2:c.2379G>A | NP_001180569.1:p.Arg793= | |
| NM_001257965.2:c.2643G>A | NP_001244894.1:p.Arg881= | |
| NR_047563.2:n.2668G>A | ||
| NR_047564.2:n.2876G>A | ||
| NM_001257966.2:c.2129-6113G>A | NP_001244895.1:n.2129-6113G>A |