Linked Data
dbSNP Id:
rs1251576341
gnomAD v2:
1-47397990-G-A
gnomAD v3:
1-46932318-G-A
gnomAD v4:
1-46932318-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.46932318G>A , CM000663.2:g.46932318G>A | GRCh38 |
| NC_000001.10:g.47397990G>A , CM000663.1:g.47397990G>A | GRCh37 |
| NC_000001.9:g.47170577G>A | NCBI36 |
| NG_007932.1:g.14167C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310638.9:c.1364+443C>T MANE Select | ENSP00000311095.4:n.1364+443C>T | |
| ENST00000310638.8:c.1364+443C>T | ENSP00000311095.4:n.1364+443C>T | |
| ENST00000371904.8:c.1367+443C>T | ENSP00000360971.4:n.1367+443C>T | |
| ENST00000462347.5:c.1070+443C>T | ENSP00000477495.1:n.1070+443C>T | |
| ENST00000465874.5:c.*605C>T | ENSP00000476368.1:n.*605C>T | |
| ENST00000468629.5:c.*69+443C>T | ENSP00000476619.1:n.*69+443C>T | |
| ENST00000474458.5:c.*69+443C>T | ENSP00000476988.1:n.*69+443C>T | |
| ENST00000475477.5:c.*158+443C>T | ENSP00000476854.1:n.*158+443C>T | |
| NM_000778.3:c.1364+443C>T | NP_000769.2:n.1364+443C>T | |
| XM_011540826.1:c.1382+443C>T | XP_011539128.1:n.1382+443C>T | |
| XM_011540827.1:c.1088+443C>T | XP_011539129.1:n.1088+443C>T | |
| XM_011540828.1:c.1070+443C>T | XP_011539130.1:n.1070+443C>T | |
| XR_246241.1:n.1268+443C>T | ||
| XR_246242.1:n.1252+443C>T | ||
| NM_001319155.1:c.1268+443C>T | NP_001306084.1:n.1268+443C>T | |
| NM_001363587.1:c.1070+443C>T | NP_001350516.1:n.1070+443C>T | |
| NR_134988.1:n.1069+443C>T | ||
| NR_134989.1:n.1260+443C>T | ||
| NR_134990.1:n.1254+443C>T | ||
| NR_134991.1:n.1241+443C>T | ||
| NR_134992.1:n.870+443C>T | ||
| NR_134993.1:n.1004+443C>T | ||
| NR_134994.1:n.1276+443C>T | ||
| XM_017000465.1:c.1052+443C>T | XP_016855954.1:n.1052+443C>T | |
| XR_001737005.1:n.1342+443C>T | ||
| NM_000778.4:c.1364+443C>T MANE Select | NP_000769.2:n.1364+443C>T | |
| NM_001319155.2:c.1268+443C>T | NP_001306084.1:n.1268+443C>T | |
| NM_001363587.2:c.1070+443C>T | NP_001350516.1:n.1070+443C>T | |
| NR_134988.2:n.1061+443C>T | ||
| NR_134989.2:n.1252+443C>T | ||
| NR_134990.2:n.1246+443C>T | ||
| NR_134991.2:n.1233+443C>T | ||
| NR_134992.2:n.862+443C>T | ||
| NR_134993.2:n.996+443C>T | ||
| NR_134994.2:n.1268+443C>T |