Linked Data
MyVariant Identifiers:
chr1:g.183177116T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.183207981T>A , CM000663.2:g.183207981T>A | GRCh38 |
| NC_000001.10:g.183177116T>A , CM000663.1:g.183177116T>A | GRCh37 |
| NC_000001.9:g.181443739T>A | NCBI36 |
| NG_007079.2:g.26718T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264144.5:c.180T>A MANE Select | ENSP00000264144.4:p.Thr60= | |
| ENST00000264144.4:c.180T>A | ENSP00000264144.4:p.Thr60= | |
| ENST00000493293.5:c.180T>A | ENSP00000432063.1:p.Thr60= | |
| NM_005562.2:c.180T>A | NP_005553.2:p.Thr60= | |
| NM_018891.2:c.180T>A | NP_061486.2:p.Thr60= | |
| XM_017001273.2:c.180T>A | XP_016856762.1:p.Thr60= | |
| NM_005562.3:c.180T>A MANE Select | NP_005553.2:p.Thr60= | |
| NM_018891.3:c.180T>A | NP_061486.2:p.Thr60= |