Linked Data
dbSNP Id:
rs1484936289
gnomAD v2:
18-50734164-T-C
gnomAD v3:
18-53207794-T-C
gnomAD v4:
18-53207794-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.53207794T>C , CM000680.2:g.53207794T>C | GRCh38 |
| NC_000018.9:g.50734164T>C , CM000680.1:g.50734164T>C | GRCh37 |
| NC_000018.8:g.48988162T>C | NCBI36 |
| NG_013341.1:g.872623T>C | |
| NG_013341.2:g.872623T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000442544.7:c.1838T>C MANE Select | ENSP00000389140.2:p.Ile613Thr | |
| ENST00000304775.12:c.1639T>C | ||
| ENST00000412726.5:c.1769T>C | ENSP00000397322.2:p.Ile590Thr | |
| ENST00000442544.6:c.1838T>C | ENSP00000389140.2:p.Ile613Thr | |
| ENST00000581580.5:c.803T>C | ENSP00000464582.1:p.Ile268Thr | |
| NM_005215.3:c.1838T>C | NP_005206.2:p.Ile613Thr | |
| XM_011525843.1:c.1838T>C | XP_011524145.1:p.Ile613Thr | |
| XM_011525844.1:c.803T>C | XP_011524146.1:p.Ile268Thr | |
| XM_011525845.1:c.1838T>C | XP_011524147.1:p.Ile613Thr | |
| XM_011525846.1:c.1838T>C | XP_011524148.1:p.Ile613Thr | |
| XM_011525844.2:c.803T>C | XP_011524146.1:p.Ile268Thr | |
| XM_017025568.1:c.1838T>C | XP_016881057.1:p.Ile613Thr | |
| XM_017025569.1:c.1838T>C | XP_016881058.1:p.Ile613Thr | |
| XM_017025570.1:c.803T>C | XP_016881059.1:p.Ile268Thr | |
| NM_005215.4:c.1838T>C MANE Select | NP_005206.2:p.Ile613Thr |