Linked Data
MyVariant Identifiers:
chr5:g.135382049G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.136046360G>A , CM000667.2:g.136046360G>A | GRCh38 |
| NC_000005.9:g.135382049G>A , CM000667.1:g.135382049G>A | GRCh37 |
| NC_000005.8:g.135409948G>A | NCBI36 |
| NG_012646.1:g.22466G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000442011.7:c.324G>A MANE Select | ENSP00000416330.2:p.Glu108= | |
| ENST00000442011.6:c.324G>A | ENSP00000416330.2:p.Glu108= | |
| ENST00000504185.5:n.481G>A | ||
| ENST00000506699.5:n.389G>A | ||
| ENST00000507018.5:c.241G>A | ||
| ENST00000515433.1:n.616G>A | ||
| NM_000358.2:c.324G>A | NP_000349.1:p.Glu108= | |
| NM_000358.3:c.324G>A MANE Select | NP_000349.1:p.Glu108= |