Linked Data
gnomAD v4:
19-55154527-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154527C>T , CM000681.2:g.55154527C>T | GRCh38 |
| NC_000019.9:g.55665895C>T , CM000681.1:g.55665895C>T | GRCh37 |
| NC_000019.8:g.60357707C>T | NCBI36 |
| NG_007866.2:g.8206G>A , LRG_432:g.8206G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.372+214G>A MANE Select | ENSP00000341838.5:n.372+214G>A | |
| ENST00000665070.1:c.405+181G>A | ENSP00000499482.1:n.405+181G>A | |
| ENST00000344887.9:c.372+214G>A | ENSP00000341838.5:n.372+214G>A | |
| ENST00000585806.5:n.371+214G>A | ||
| ENST00000586669.5:n.380+214G>A | ||
| ENST00000587176.5:n.770G>A | ||
| ENST00000588882.1:c.297+214G>A | ENSP00000466729.1:n.297+214G>A | |
| NM_000363.4:c.372+214G>A , LRG_432t1:c.372+214G>A | NP_000354.4:n.372+214G>A | |
| NM_000363.5:c.372+214G>A MANE Select | NP_000354.4:n.372+214G>A |