Linked Data
dbSNP Id:
rs2140878833
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.22825317T>A , CM000677.2:g.22825317T>A | GRCh38 |
| NC_000015.9:g.23047751A>T , CM000677.1:g.23047751A>T | GRCh37 |
| NC_000015.8:g.20599192A>T | NCBI36 |
| NG_009056.1:g.44093T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000337435.9:c.*1078T>A MANE Select | ENSP00000337452.4:n.*1078T>A | |
| ENST00000337435.8:c.*1078T>A | ENSP00000337452.4:n.*1078T>A | |
| ENST00000437912.6:c.*1078T>A | ENSP00000393962.2:n.*1078T>A | |
| ENST00000559448.5:c.2040T>A | ||
| NM_001142275.1:c.*1078T>A | NP_001135747.1:n.*1078T>A | |
| NM_144599.4:c.*1078T>A | NP_653200.2:n.*1078T>A | |
| NM_144599.5:c.*1078T>A MANE Select | NP_653200.2:n.*1078T>A |