Linked Data
gnomAD v4:
1-115738169-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115738169C>T , CM000663.2:g.115738169C>T | GRCh38 |
| NC_000001.10:g.116280790C>T , CM000663.1:g.116280790C>T | GRCh37 |
| NC_000001.9:g.116082313C>T | NCBI36 |
| NG_008802.1:g.35637G>A , LRG_404:g.35637G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000488931.2:c.256+55G>A | ENSP00000518226.1:n.256+55G>A | |
| ENST00000261448.6:c.532+55G>A MANE Select | ENSP00000261448.5:n.532+55G>A | |
| ENST00000261448.5:c.532+55G>A | ENSP00000261448.5:n.532+55G>A | |
| NM_001232.3:c.532+55G>A , LRG_404t1:c.532+55G>A | NP_001223.2:n.532+55G>A | |
| NM_001232.4:c.532+55G>A MANE Select | NP_001223.2:n.532+55G>A |