Linked Data
dbSNP Id:
rs11006747
gnomAD v2:
10-28150935-A-C
gnomAD v3:
10-27862006-A-C
gnomAD v4:
10-27862006-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.27862006A>C , CM000672.2:g.27862006A>C | GRCh38 |
| NC_000010.10:g.28150935A>C , CM000672.1:g.28150935A>C | GRCh37 |
| NC_000010.9:g.28190941A>C | NCBI36 |
| NG_042820.1:g.142045T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000305242.10:c.2799+428T>G MANE Select | ENSP00000306410.5:n.2799+428T>G | |
| ENST00000672841.1:c.1875+428T>G | ENSP00000499983.1:n.1875+428T>G | |
| ENST00000672877.1:c.1374+428T>G | ENSP00000500120.1:n.1374+428T>G | |
| ENST00000673384.1:c.1875+428T>G | ENSP00000500856.1:n.1875+428T>G | |
| ENST00000673439.1:c.2799+428T>G | ENSP00000500782.1:n.2799+428T>G | |
| ENST00000305242.9:c.2799+428T>G | ENSP00000306410.5:n.2799+428T>G | |
| NM_001290020.1:c.2799+428T>G | NP_001276949.1:n.2799+428T>G | |
| NM_001290021.1:c.1374+428T>G | NP_001276950.1:n.1374+428T>G | |
| NM_001312689.1:c.1875+428T>G | NP_001299618.1:n.1875+428T>G | |
| NM_018076.3:c.2799+428T>G | NP_060546.2:n.2799+428T>G | |
| NM_018076.4:c.2799+428T>G | NP_060546.2:n.2799+428T>G | |
| XM_011519526.1:c.2799+428T>G | XP_011517828.1:n.2799+428T>G | |
| XM_011519527.1:c.2799+428T>G | XP_011517829.1:n.2799+428T>G | |
| XM_011519528.1:c.2799+428T>G | XP_011517830.1:n.2799+428T>G | |
| XM_011519529.1:c.2799+428T>G | XP_011517831.1:n.2799+428T>G | |
| XM_011519530.1:c.2799+428T>G | XP_011517832.1:n.2799+428T>G | |
| XM_011519531.1:c.2799+428T>G | XP_011517833.1:n.2799+428T>G | |
| XM_011519532.1:c.2589+428T>G | XP_011517834.1:n.2589+428T>G | |
| XM_011519533.1:c.1875+428T>G | XP_011517835.1:n.1875+428T>G | |
| XM_011519534.1:c.1875+428T>G | XP_011517836.1:n.1875+428T>G | |
| XM_011519535.1:c.1713+428T>G | XP_011517837.1:n.1713+428T>G | |
| XM_011519537.1:c.1374+428T>G | XP_011517839.1:n.1374+428T>G | |
| XM_024448049.1:c.2928+428T>G | XP_024303817.1:n.2928+428T>G | |
| XM_024448050.1:c.2928+428T>G | XP_024303818.1:n.2928+428T>G | |
| XM_024448051.1:c.2928+428T>G | XP_024303819.1:n.2928+428T>G | |
| XM_024448052.1:c.2928+428T>G | XP_024303820.1:n.2928+428T>G | |
| XM_024448053.1:c.2928+428T>G | XP_024303821.1:n.2928+428T>G | |
| XM_024448054.1:c.2718+428T>G | XP_024303822.1:n.2718+428T>G | |
| XM_024448055.1:c.2004+428T>G | XP_024303823.1:n.2004+428T>G | |
| XM_024448056.1:c.2004+428T>G | XP_024303824.1:n.2004+428T>G | |
| XM_024448057.1:c.1842+428T>G | XP_024303825.1:n.1842+428T>G | |
| XM_024448058.1:c.1503+428T>G | XP_024303826.1:n.1503+428T>G | |
| NM_001290020.2:c.2799+428T>G | NP_001276949.1:n.2799+428T>G | |
| NM_001290021.2:c.1374+428T>G | NP_001276950.1:n.1374+428T>G | |
| NM_001312689.2:c.1875+428T>G | NP_001299618.1:n.1875+428T>G | |
| NM_018076.5:c.2799+428T>G MANE Select | NP_060546.2:n.2799+428T>G |