Linked Data
gnomAD v4:
4-42963259-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.42963259C>G , CM000666.2:g.42963259C>G | GRCh38 |
| NC_000004.11:g.42965276C>G , CM000666.1:g.42965276C>G | GRCh37 |
| NC_000004.10:g.42660033C>G | NCBI36 |
| NG_027718.1:g.74994C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000399770.3:c.627+125C>G MANE Select | ENSP00000382670.2:n.627+125C>G | |
| ENST00000399770.2:c.627+125C>G | ENSP00000382670.2:n.627+125C>G | |
| NM_001080476.2:c.627+125C>G | NP_001073945.1:n.627+125C>G | |
| XM_011513691.1:c.264+125C>G | XP_011511993.1:n.264+125C>G | |
| NM_001080476.3:c.627+125C>G MANE Select | NP_001073945.1:n.627+125C>G |