Linked Data
gnomAD v4:
6-143485261-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.143485261C>A , CM000668.2:g.143485261C>A | GRCh38 |
| NC_000006.11:g.143806398C>A , CM000668.1:g.143806398C>A | GRCh37 |
| NC_000006.10:g.143848091C>A | NCBI36 |
| NG_008459.1:g.39481C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367591.5:c.1038+13C>A MANE Select | ENSP00000356563.4:n.1038+13C>A | |
| ENST00000367591.4:c.1038+13C>A | ENSP00000356563.4:n.1038+13C>A | |
| ENST00000585848.1:n.177+13C>A | ||
| NM_003630.2:c.1038+13C>A | NP_003621.1:n.1038+13C>A | |
| NM_003630.3:c.1038+13C>A MANE Select | NP_003621.1:n.1038+13C>A |