Linked Data
gnomAD v4:
4-42963237-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.42963237C>T , CM000666.2:g.42963237C>T | GRCh38 |
| NC_000004.11:g.42965254C>T , CM000666.1:g.42965254C>T | GRCh37 |
| NC_000004.10:g.42660011C>T | NCBI36 |
| NG_027718.1:g.74972C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000399770.3:c.627+103C>T MANE Select | ENSP00000382670.2:n.627+103C>T | |
| ENST00000399770.2:c.627+103C>T | ENSP00000382670.2:n.627+103C>T | |
| NM_001080476.2:c.627+103C>T | NP_001073945.1:n.627+103C>T | |
| XM_011513691.1:c.264+103C>T | XP_011511993.1:n.264+103C>T | |
| NM_001080476.3:c.627+103C>T MANE Select | NP_001073945.1:n.627+103C>T |