Linked Data
gnomAD v4:
6-143485257-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.143485257A>G , CM000668.2:g.143485257A>G | GRCh38 |
| NC_000006.11:g.143806394A>G , CM000668.1:g.143806394A>G | GRCh37 |
| NC_000006.10:g.143848087A>G | NCBI36 |
| NG_008459.1:g.39477A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367591.5:c.1038+9A>G MANE Select | ENSP00000356563.4:n.1038+9A>G | |
| ENST00000367591.4:c.1038+9A>G | ENSP00000356563.4:n.1038+9A>G | |
| ENST00000585848.1:n.177+9A>G | ||
| NM_003630.2:c.1038+9A>G | NP_003621.1:n.1038+9A>G | |
| NM_003630.3:c.1038+9A>G MANE Select | NP_003621.1:n.1038+9A>G |