Linked Data
gnomAD v4:
1-115738173-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115738173G>T , CM000663.2:g.115738173G>T | GRCh38 |
| NC_000001.10:g.116280794G>T , CM000663.1:g.116280794G>T | GRCh37 |
| NC_000001.9:g.116082317G>T | NCBI36 |
| NG_008802.1:g.35633C>A , LRG_404:g.35633C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000488931.2:c.256+51C>A | ENSP00000518226.1:n.256+51C>A | |
| ENST00000261448.6:c.532+51C>A MANE Select | ENSP00000261448.5:n.532+51C>A | |
| ENST00000261448.5:c.532+51C>A | ENSP00000261448.5:n.532+51C>A | |
| NM_001232.3:c.532+51C>A , LRG_404t1:c.532+51C>A | NP_001223.2:n.532+51C>A | |
| NM_001232.4:c.532+51C>A MANE Select | NP_001223.2:n.532+51C>A |