Linked Data
dbSNP Id:
rs1180734423
gnomAD v2:
2-32353307-G-A
gnomAD v3:
2-32128238-G-A
gnomAD v4:
2-32128238-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.32128238G>A , CM000664.2:g.32128238G>A | GRCh38 |
| NC_000002.11:g.32353307G>A , CM000664.1:g.32353307G>A | GRCh37 |
| NC_000002.10:g.32206811G>A | NCBI36 |
| NG_008730.1:g.69628G>A , LRG_714:g.69628G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000704289.1:c.*834-170G>A | ENSP00000515816.1:n.*834-170G>A | |
| ENST00000315285.9:c.1174-170G>A MANE Select | ENSP00000320885.3:n.1174-170G>A | |
| ENST00000621856.2:c.1171-170G>A | ENSP00000482496.2:n.1171-170G>A | |
| ENST00000642281.1:c.983-8325G>A | ||
| ENST00000642455.1:c.1075-170G>A | ENSP00000493827.1:n.1075-170G>A | |
| ENST00000642751.1:c.948-170G>A | ||
| ENST00000642999.1:c.916-170G>A | ENSP00000496589.1:n.916-170G>A | |
| ENST00000643327.1:c.333-170G>A | ||
| ENST00000643334.1:c.754-170G>A | ||
| ENST00000644408.1:c.1050-170G>A | ||
| ENST00000644954.1:c.820-170G>A | ENSP00000494312.1:n.820-170G>A | |
| ENST00000645159.1:n.1741G>A | ||
| ENST00000645550.1:n.387-170G>A | ||
| ENST00000645671.1:c.624-170G>A | ||
| ENST00000645730.1:c.521-170G>A | ||
| ENST00000646082.1:c.820-170G>A | ||
| ENST00000646571.1:c.1078-170G>A | ENSP00000495015.1:n.1078-170G>A | |
| ENST00000647007.1:n.866-170G>A | ||
| ENST00000647133.1:c.674-170G>A | ||
| ENST00000315285.7:c.1174-170G>A | ENSP00000320885.3:n.1174-170G>A | |
| ENST00000345662.5:c.1078-170G>A | ENSP00000340817.1:n.1078-170G>A | |
| ENST00000615843.4:c.1174-170G>A | ENSP00000480893.1:n.1174-170G>A | |
| ENST00000621856.1:c.916-170G>A | ENSP00000482496.1:n.916-170G>A | |
| NM_014946.3:c.1174-170G>A , LRG_714t1:c.1174-170G>A | NP_055761.2:n.1174-170G>A | |
| NM_199436.1:c.1078-170G>A | NP_955468.1:n.1078-170G>A | |
| XM_005264516.3:c.1171-170G>A | XP_005264573.1:n.1171-170G>A | |
| XM_011533067.1:c.1174-170G>A | XP_011531369.1:n.1174-170G>A | |
| NM_001363823.1:c.1171-170G>A | NP_001350752.1:n.1171-170G>A | |
| NM_001363875.1:c.1075-170G>A | NP_001350804.1:n.1075-170G>A | |
| XM_005264516.5:c.1171-170G>A | XP_005264573.1:n.1171-170G>A | |
| XM_011533067.2:c.1174-170G>A | XP_011531369.1:n.1174-170G>A | |
| XM_017004778.2:c.1078-170G>A | XP_016860267.1:n.1078-170G>A | |
| NM_001363823.2:c.1171-170G>A | NP_001350752.1:n.1171-170G>A | |
| NM_001363875.2:c.1075-170G>A | NP_001350804.1:n.1075-170G>A | |
| NM_001377959.1:c.1078-170G>A | NP_001364888.1:n.1078-170G>A | |
| NM_014946.4:c.1174-170G>A MANE Select | NP_055761.2:n.1174-170G>A | |
| NM_199436.2:c.1078-170G>A | NP_955468.1:n.1078-170G>A |