Linked Data
gnomAD v4:
12-63146873-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.63146873A>C , CM000674.2:g.63146873A>C | GRCh38 |
| NC_000012.11:g.63540653A>C , CM000674.1:g.63540653A>C | GRCh37 |
| NC_000012.10:g.61826920A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299178.4:c.*486T>G MANE Select | ENSP00000299178.3:n.*486T>G | |
| ENST00000299178.3:c.*486T>G | ENSP00000299178.2:n.*486T>G | |
| ENST00000550940.1:c.538+548T>G | ENSP00000449822.1:n.538+548T>G | |
| NM_000706.4:c.*486T>G | NP_000697.1:n.*486T>G | |
| XM_005269002.3:c.*486T>G | XP_005269059.1:n.*486T>G | |
| NM_000706.5:c.*486T>G MANE Select | NP_000697.1:n.*486T>G |