Linked Data
MyVariant Identifiers:
chr9:g.133748266C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.130872879C>G , CM000671.2:g.130872879C>G | GRCh38 |
| NC_000009.11:g.133748266C>G , CM000671.1:g.133748266C>G | GRCh37 |
| NC_000009.10:g.132738087C>G | NCBI36 |
| NG_012034.1:g.163999C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372348.9:c.984C>G | ENSP00000361423.2:p.Pro328= | |
| ENST00000318560.6:c.927C>G MANE Select | ENSP00000323315.5:p.Pro309= | |
| ENST00000372348.7:c.984C>G | ENSP00000361423.2:p.Pro328= | |
| ENST00000318560.5:c.927C>G | ENSP00000323315.5:p.Pro309= | |
| ENST00000372348.6:c.984C>G | ENSP00000361423.2:p.Pro328= | |
| NM_005157.5:c.927C>G | NP_005148.2:p.Pro309= | |
| NM_007313.2:c.984C>G | NP_009297.2:p.Pro328= | |
| NM_005157.6:c.927C>G MANE Select | NP_005148.2:p.Pro309= | |
| NM_007313.3:c.984C>G | NP_009297.2:p.Pro328= |