Linked Data
dbSNP Id:
rs574955582
gnomAD v2:
12-80849462-T-C
gnomAD v3:
12-80460715-A-G
gnomAD v4:
12-80460715-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.80460715A>G , CM000674.2:g.80460715A>G | GRCh38 |
| NC_000012.11:g.80849462T>C , CM000674.1:g.80849462T>C | GRCh37 |
| NC_000012.10:g.79373593T>C | NCBI36 |
| NG_034052.1:g.21370A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644991.3:c.723A>G MANE Select | ENSP00000495607.1:p.Thr241= | |
| ENST00000614701.4:c.723A>G | ENSP00000482885.1:p.Thr241= | |
| ENST00000616559.4:c.849A>G | ENSP00000483259.1:p.Thr283= | |
| NM_001145026.1:c.723A>G | NP_001138498.1:p.Thr241= | |
| XM_011538290.1:c.723A>G | XP_011536592.1:p.Thr241= | |
| XM_017019273.1:c.1389A>G | XP_016874762.1:p.Thr463= | |
| XM_017019274.1:c.1389A>G | XP_016874763.1:p.Thr463= | |
| XM_017019275.1:c.1389A>G | XP_016874764.1:p.Thr463= | |
| XR_001748688.1:n.1526A>G | ||
| XR_001748689.1:n.1526A>G | ||
| NM_001145026.2:c.723A>G MANE Select | NP_001138498.1:p.Thr241= |