Linked Data
gnomAD v4:
8-63072912-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.63072912A>T , CM000670.2:g.63072912A>T | GRCh38 |
| NC_000008.10:g.63985471A>T , CM000670.1:g.63985471A>T | GRCh37 |
| NC_000008.9:g.64148025A>T | NCBI36 |
| NG_016123.1:g.18142T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260116.5:c.358+23T>A MANE Select | ENSP00000260116.4:n.358+23T>A | |
| ENST00000260116.4:c.358+23T>A | ENSP00000260116.4:n.358+23T>A | |
| ENST00000521138.1:n.232+12906T>A | ||
| NM_000370.3:c.358+23T>A MANE Select | NP_000361.1:n.358+23T>A | |
| XM_006716468.2:c.205-8596T>A | XP_006716531.1:n.205-8596T>A | |
| XM_006716468.4:c.205-8596T>A | XP_006716531.1:n.205-8596T>A |