Linked Data
MyVariant Identifiers:
chr5:g.1416227G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1416112G>C , CM000667.2:g.1416112G>C | GRCh38 |
| NC_000005.9:g.1416227G>C , CM000667.1:g.1416227G>C | GRCh37 |
| NC_000005.8:g.1469227G>C | NCBI36 |
| NG_015885.1:g.34317C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270349.12:c.1017C>G MANE Select | ENSP00000270349.9:p.Thr339= | |
| ENST00000270349.11:c.1017C>G | ENSP00000270349.9:p.Thr339= | |
| ENST00000511750.1:n.467C>G | ||
| NM_001044.4:c.1017C>G | NP_001035.1:p.Thr339= | |
| NM_001044.5:c.1017C>G MANE Select | NP_001035.1:p.Thr339= |