Linked Data
MyVariant Identifiers:
chr17:g.7357827T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7454508T>C , CM000679.2:g.7454508T>C | GRCh38 |
| NC_000017.10:g.7357827T>C , CM000679.1:g.7357827T>C | GRCh37 |
| NC_000017.9:g.7298551T>C | NCBI36 |
| NG_008026.1:g.14422T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306071.7:c.1032T>C MANE Select | ENSP00000304290.2:p.Leu344= | |
| ENST00000306071.6:c.1032T>C | ENSP00000304290.2:p.Leu344= | |
| ENST00000536404.6:c.816T>C | ENSP00000439209.2:p.Leu272= | |
| ENST00000570557.5:c.695T>C | ||
| ENST00000573209.1:n.1976T>C | ||
| ENST00000576360.1:c.669T>C | ENSP00000459092.1:p.Leu223= | |
| NM_000747.2:c.1032T>C | NP_000738.2:p.Leu344= | |
| NM_000747.3:c.1032T>C MANE Select | NP_000738.2:p.Leu344= |