Linked Data
MyVariant Identifiers:
chr14:g.101349359T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.100883022T>C , CM000676.2:g.100883022T>C | GRCh38 |
| NC_000014.8:g.101349359T>C , CM000676.1:g.101349359T>C | GRCh37 |
| NC_000014.7:g.100419112T>C | NCBI36 |
| NG_045001.1:g.6826A>G | |
| NG_045000.5:g.51754T>C | |
| NG_045000.6:g.51754T>C | |
| NG_045001.2:g.25701A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649591.1:c.1767A>G (RTL1) MANE Select | ENSP00000497482.1:p.Glu589= | |
| ENST00000534062.1:c.1767A>G (RTL1) | ENSP00000435342.1:p.Glu589= | |
| NM_001134888.2:c.1767A>G (RTL1) | NP_001128360.1:p.Glu589= | |
| NR_029696.1:n.44T>C (MIR127) | ||
| NM_001134888.3:c.1767A>G (RTL1) MANE Select | NP_001128360.1:p.Glu589= |