Linked Data
MyVariant Identifiers:
chr9:g.131707969G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.128945690G>T , CM000671.2:g.128945690G>T | GRCh38 |
| NC_000009.11:g.131707969G>T , CM000671.1:g.131707969G>T | GRCh37 |
| NC_000009.10:g.130747790G>T | NCBI36 |
| NG_017009.1:g.7044C>A , LRG_744:g.7044C>A | |
| NG_033111.1:g.2998G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372586.4:c.1614C>A MANE Select | ENSP00000361667.3:p.Ala538= | |
| ENST00000372586.3:c.1614C>A | ENSP00000361667.3:p.Ala538= | |
| ENST00000482796.1:c.39-3499G>T | ENSP00000417556.2:n.39-3499G>T | |
| NM_014908.3:c.1614C>A , LRG_744t1:c.1614C>A | NP_055723.1:p.Ala538= | |
| NM_014908.4:c.1614C>A MANE Select | NP_055723.1:p.Ala538= |