Linked Data
dbSNP Id:
rs774212140
ExAC:
7:150555829 C / T
gnomAD v2:
7-150555829-C-T
gnomAD v3:
7-150858741-C-T
gnomAD v4:
7-150858741-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150858741C>T , CM000669.2:g.150858741C>T | GRCh38 |
| NC_000007.13:g.150555829C>T , CM000669.1:g.150555829C>T | GRCh37 |
| NC_000007.12:g.150186762C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360937.9:c.1571-22C>T MANE Select | ENSP00000354193.4:n.1571-22C>T | |
| ENST00000360937.8:c.1571-22C>T | ENSP00000354193.4:n.1571-22C>T | |
| ENST00000416793.6:c.1571-22C>T | ENSP00000411613.2:n.1571-22C>T | |
| ENST00000467291.5:c.1571-22C>T | ENSP00000418328.1:n.1571-22C>T | |
| ENST00000480582.1:n.109-22C>T | ||
| ENST00000493429.5:c.1571-22C>T | ENSP00000418614.1:n.1571-22C>T | |
| ENST00000619575.1:c.1565-22C>T | ENSP00000481717.1:n.1565-22C>T | |
| ENST00000622116.4:c.149-22C>T | ENSP00000481520.1:n.149-22C>T | |
| NM_001091.3:c.1571-22C>T | NP_001082.2:n.1571-22C>T | |
| NM_001272072.1:c.1571-22C>T | NP_001259001.1:n.1571-22C>T | |
| XM_011516008.1:c.1571-22C>T | XP_011514310.1:n.1571-22C>T | |
| XM_011516009.1:c.1571-22C>T | XP_011514311.1:n.1571-22C>T | |
| XR_928169.1:n.296-17296G>A | ||
| XR_928170.1:n.425+9875G>A | ||
| XR_928171.1:n.298-17296G>A | ||
| XM_017011944.1:c.1571-22C>T | XP_016867433.1:n.1571-22C>T | |
| XM_017011945.1:c.1571-22C>T | XP_016867434.1:n.1571-22C>T | |
| XM_017011946.2:c.1571-22C>T | XP_016867435.1:n.1571-22C>T | |
| XM_017011947.1:c.1571-22C>T | XP_016867436.1:n.1571-22C>T | |
| XR_928169.2:n.302-17296G>A | ||
| XR_928171.2:n.302-17296G>A | ||
| NM_001091.4:c.1571-22C>T MANE Select | NP_001082.2:n.1571-22C>T | |
| NM_001272072.2:c.1571-22C>T | NP_001259001.1:n.1571-22C>T |