Linked Data
MyVariant Identifiers:
chr10:g.73767560G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.72007802G>T , CM000672.2:g.72007802G>T | GRCh38 |
| NC_000010.10:g.73767560G>T , CM000672.1:g.73767560G>T | GRCh37 |
| NC_000010.9:g.73437566G>T | NCBI36 |
| NG_012635.1:g.48441G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373115.5:c.771G>T MANE Select | ENSP00000362207.4:p.Val257= | |
| ENST00000373115.4:c.771G>T | ENSP00000362207.4:p.Val257= | |
| NM_004273.4:c.771G>T | NP_004264.2:p.Val257= | |
| XM_006718075.2:c.771G>T | XP_006718138.1:p.Val257= | |
| XM_011540369.1:c.771G>T | XP_011538671.1:p.Val257= | |
| XM_006718075.4:c.771G>T | XP_006718138.1:p.Val257= | |
| XM_011540369.2:c.771G>T | XP_011538671.1:p.Val257= | |
| NM_004273.5:c.771G>T MANE Select | NP_004264.2:p.Val257= |