Linked Data
dbSNP Id:
rs1276281854
gnomAD v2:
4-73179441-T-C
gnomAD v3:
4-72313724-T-C
gnomAD v4:
4-72313724-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.72313724T>C , CM000666.2:g.72313724T>C | GRCh38 |
| NC_000004.11:g.73179441T>C , CM000666.1:g.73179441T>C | GRCh37 |
| NC_000004.10:g.73398305T>C | NCBI36 |
| NG_046955.1:g.260076A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286657.10:c.1698A>G MANE Select | ENSP00000286657.4:p.Thr566= | |
| ENST00000286657.8:c.1698A>G | ENSP00000286657.4:p.Thr566= | |
| ENST00000622135.1:c.1698A>G | ENSP00000480055.1:p.Thr566= | |
| NM_014243.2:c.1698A>G | NP_055058.2:p.Thr566= | |
| XM_011532421.1:c.1641A>G | XP_011530723.1:p.Thr547= | |
| XM_011532422.1:c.1614A>G | XP_011530724.1:p.Thr538= | |
| XM_011532423.1:c.1056A>G | XP_011530725.1:p.Thr352= | |
| XM_011532424.1:c.966A>G | XP_011530726.1:p.Thr322= | |
| XM_011532421.2:c.1641A>G | XP_011530723.1:p.Thr547= | |
| XM_011532422.3:c.1614A>G | XP_011530724.1:p.Thr538= | |
| NM_014243.3:c.1698A>G MANE Select | NP_055058.2:p.Thr566= |