Linked Data
dbSNP Id:
rs772333285
ExAC:
15:89861882 G / T
gnomAD v2:
15-89861882-G-T
gnomAD v4:
15-89318651-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.89318651G>T , CM000677.2:g.89318651G>T | GRCh38 |
| NC_000015.9:g.89861882G>T , CM000677.1:g.89861882G>T | GRCh37 |
| NC_000015.8:g.87662886G>T | NCBI36 |
| NG_008218.1:g.21145C>A | |
| NG_011736.1:g.79689G>T , LRG_500:g.79689G>T | |
| NG_008218.2:g.21145C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000636937.2:c.3372C>A | ENSP00000516154.1:p.Ala1124= | |
| ENST00000268124.11:c.3372C>A MANE Select | ENSP00000268124.5:p.Ala1124= | |
| ENST00000530292.3:c.2973C>A | ENSP00000432885.2:p.Ala991= | |
| ENST00000635986.2:c.*442C>A | ENSP00000490653.2:n.*442C>A | |
| ENST00000636774.1:c.*1939C>A | ENSP00000489799.1:n.*1939C>A | |
| ENST00000637238.1:c.2181C>A | ENSP00000490756.1:n.2181C>A | |
| ENST00000637264.1:c.2444C>A | ||
| ENST00000666746.1:c.2949C>A | ||
| ENST00000672071.1:n.3570C>A | ||
| ENST00000672695.1:n.549C>A | ||
| ENST00000672923.2:n.3372C>A | ||
| ENST00000268124.9:c.3372C>A | ENSP00000268124.5:p.Ala1124= | |
| ENST00000442287.6:c.3372C>A | ENSP00000399851.2:p.Ala1124= | |
| ENST00000530292.2:c.456C>A | ENSP00000432885.1:p.Ala152= | |
| ENST00000631044.2:c.*2796C>A | ENSP00000486730.1:n.*2796C>A | |
| NM_001126131.1:c.3372C>A | NP_001119603.1:p.Ala1124= | |
| NM_002693.2:c.3372C>A | NP_002684.1:p.Ala1124= | |
| NM_001126131.2:c.3372C>A | NP_001119603.1:p.Ala1124= | |
| NM_002693.3:c.3372C>A MANE Select | NP_002684.1:p.Ala1124= |