Linked Data
gnomAD v4:
1-160139494-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160139494A>T , CM000663.2:g.160139494A>T | GRCh38 |
| NC_000001.10:g.160109284A>T , CM000663.1:g.160109284A>T | GRCh37 |
| NC_000001.9:g.158375908A>T | NCBI36 |
| NG_008014.1:g.28737A>T , LRG_6:g.28737A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361216.8:c.2841-146A>T MANE Select | ENSP00000354490.3:n.2841-146A>T | |
| ENST00000361216.7:c.2841-146A>T | ENSP00000354490.3:n.2841-146A>T | |
| ENST00000392233.7:c.2841-146A>T | ENSP00000376066.3:n.2841-146A>T | |
| ENST00000447527.1:c.1922-146A>T | ||
| ENST00000463989.1:n.177-146A>T | ||
| NM_000702.3:c.2841-146A>T | NP_000693.1:n.2841-146A>T | |
| NM_000702.4:c.2841-146A>T MANE Select | NP_000693.1:n.2841-146A>T |