Linked Data
gnomAD v4:
19-55154016-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154016T>C , CM000681.2:g.55154016T>C | GRCh38 |
| NC_000019.9:g.55665384T>C , CM000681.1:g.55665384T>C | GRCh37 |
| NC_000019.8:g.60357196T>C | NCBI36 |
| NG_007866.2:g.8717A>G , LRG_432:g.8717A>G | |
| NG_011829.2:g.223A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.549+14A>G MANE Select | ENSP00000341838.5:n.549+14A>G | |
| ENST00000665070.1:c.582+14A>G | ENSP00000499482.1:n.582+14A>G | |
| ENST00000344887.9:c.549+14A>G | ENSP00000341838.5:n.549+14A>G | |
| ENST00000585806.5:n.548+14A>G | ||
| ENST00000588882.1:c.474+14A>G | ENSP00000466729.1:n.474+14A>G | |
| ENST00000589864.1:n.377+14A>G | ||
| NM_000363.4:c.549+14A>G , LRG_432t1:c.549+14A>G | NP_000354.4:n.549+14A>G | |
| NM_000363.5:c.549+14A>G MANE Select | NP_000354.4:n.549+14A>G |