Linked Data
dbSNP Id:
rs755310512
gnomAD v2:
10-44068477-C-T
gnomAD v3:
10-43573029-C-T
gnomAD v4:
10-43573029-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.43573029C>T , CM000672.2:g.43573029C>T | GRCh38 |
| NC_000010.10:g.44068477C>T , CM000672.1:g.44068477C>T | GRCh37 |
| NC_000010.9:g.43388483C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000374446.7:c.-216+608G>A MANE Select | ENSP00000363569.1:n.-216+608G>A | |
| ENST00000374446.6:c.-216+608G>A | ENSP00000363569.1:n.-216+608G>A | |
| ENST00000426961.1:c.-216+1511G>A | ENSP00000398202.1:n.-216+1511G>A | |
| ENST00000491188.1:n.58+1511G>A | ||
| ENST00000535642.5:c.-93+1511G>A | ENSP00000443907.1:n.-93+1511G>A | |
| NM_001099282.1:c.-216+608G>A | NP_001092752.1:n.-216+608G>A | |
| NM_001099283.1:c.-93+1511G>A | NP_001092753.1:n.-93+1511G>A | |
| NM_001099284.1:c.-216+1511G>A | NP_001092754.1:n.-216+1511G>A | |
| XM_005271828.1:c.-216+608G>A | XP_005271885.1:n.-216+608G>A | |
| XM_005271829.1:c.-216+1442G>A | XP_005271886.1:n.-216+1442G>A | |
| XM_005271831.1:c.-93+1442G>A | XP_005271888.1:n.-93+1442G>A | |
| XM_006718002.1:c.-93+608G>A | XP_006718065.1:n.-93+608G>A | |
| XM_006718003.2:c.-93+1009G>A | XP_006718066.1:n.-93+1009G>A | |
| XM_011540233.1:c.-94+608G>A | XP_011538535.1:n.-94+608G>A | |
| XM_011540234.1:c.-94+1511G>A | XP_011538536.1:n.-94+1511G>A | |
| XM_011540235.1:c.-94+1442G>A | XP_011538537.1:n.-94+1442G>A | |
| XM_011540236.1:c.-94+1009G>A | XP_011538538.1:n.-94+1009G>A | |
| NM_001324347.1:c.-93+608G>A | NP_001311276.1:n.-93+608G>A | |
| NM_001324348.1:c.-93+1442G>A | NP_001311277.1:n.-93+1442G>A | |
| NM_001324349.1:c.-216+608G>A | NP_001311278.1:n.-216+608G>A | |
| NM_001324350.1:c.-93+608G>A | NP_001311279.1:n.-93+608G>A | |
| NM_001324351.1:c.-216+1442G>A | NP_001311280.1:n.-216+1442G>A | |
| NM_001324352.1:c.-94+608G>A | NP_001311281.1:n.-94+608G>A | |
| NM_001324353.1:c.15+608G>A | NP_001311282.1:n.15+608G>A | |
| XM_006718003.3:c.-93+1009G>A | XP_006718066.1:n.-93+1009G>A | |
| XM_011540232.3:c.-2639G>A | XP_011538534.1:n.-2639G>A | |
| XM_011540234.2:c.-94+1511G>A | XP_011538536.1:n.-94+1511G>A | |
| XM_011540235.2:c.-94+1442G>A | XP_011538537.1:n.-94+1442G>A | |
| XM_011540236.2:c.-94+1009G>A | XP_011538538.1:n.-94+1009G>A | |
| XM_017016740.1:c.-94+608G>A | XP_016872229.1:n.-94+608G>A | |
| NM_001099282.2:c.-216+608G>A MANE Select | NP_001092752.1:n.-216+608G>A | |
| NM_001324347.2:c.-93+608G>A | NP_001311276.1:n.-93+608G>A | |
| NM_001324348.2:c.-93+1442G>A | NP_001311277.1:n.-93+1442G>A | |
| NM_001324349.2:c.-216+608G>A | NP_001311278.1:n.-216+608G>A | |
| NM_001324350.2:c.-93+608G>A | NP_001311279.1:n.-93+608G>A | |
| NM_001324351.2:c.-216+1442G>A | NP_001311280.1:n.-216+1442G>A | |
| NM_001324352.2:c.-94+608G>A | NP_001311281.1:n.-94+608G>A | |
| NM_001324353.2:c.15+608G>A | NP_001311282.1:n.15+608G>A | |
| NM_001099283.2:c.-93+1511G>A | NP_001092753.1:n.-93+1511G>A | |
| NM_001099284.2:c.-216+1511G>A | NP_001092754.1:n.-216+1511G>A |