Linked Data
gnomAD v4:
6-31125775-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31125775C>A , CM000668.2:g.31125775C>A | GRCh38 |
| NC_000006.11:g.31093552C>A , CM000668.1:g.31093552C>A | GRCh37 |
| NC_000006.10:g.31201531C>A | NCBI36 |
| NG_021348.1:g.15945C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259881.10:c.-129C>A MANE Select | ENSP00000259881.9:n.-129C>A | |
| ENST00000259881.9:c.-129C>A | ENSP00000259881.9:n.-129C>A | |
| ENST00000479581.5:n.61+10884C>A | ||
| ENST00000548049.1:n.216C>A | ||
| ENST00000550838.1:n.95C>A | ||
| ENST00000552747.1:n.53+10884C>A | ||
| NM_014068.2:c.-129C>A | NP_054787.2:n.-129C>A | |
| NM_014068.3:c.-129C>A MANE Select | NP_054787.2:n.-129C>A |