Linked Data
dbSNP Id:
rs749846585
ExAC:
7:143029841 A / G
gnomAD v2:
7-143029841-A-G
gnomAD v4:
7-143332748-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.143332748A>G , CM000669.2:g.143332748A>G | GRCh38 |
| NC_000007.13:g.143029841A>G , CM000669.1:g.143029841A>G | GRCh37 |
| NC_000007.12:g.142739963A>G | NCBI36 |
| NG_009815.1:g.21623A>G | |
| NG_009815.2:g.21623A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650516.2:c.1276A>G | ENSP00000498052.2:p.Thr426Ala | |
| ENST00000343257.7:c.1276A>G MANE Select | ENSP00000339867.2:p.Thr426Ala | |
| ENST00000432192.6:c.1100A>G | ||
| ENST00000343257.6:c.1276A>G | ENSP00000339867.2:p.Thr426Ala | |
| NM_000083.2:c.1276A>G | NP_000074.2:p.Thr426Ala | |
| NR_046453.1:n.1341+245A>G | ||
| XM_011515781.1:c.1300A>G | XP_011514083.1:p.Thr434Ala | |
| XM_011515782.1:c.22A>G | XP_011514084.1:p.Thr8Ala | |
| XM_011515782.2:c.22A>G | XP_011514084.1:p.Thr8Ala | |
| XM_017011739.1:c.850A>G | XP_016867228.1:p.Thr284Ala | |
| XM_017011740.1:c.826A>G | XP_016867229.1:p.Thr276Ala | |
| NM_000083.3:c.1276A>G MANE Select | NP_000074.3:p.Thr426Ala | |
| NR_046453.2:n.1356+245A>G |