Linked Data
gnomAD v4:
19-1103993-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1103993C>A , CM000681.2:g.1103993C>A | GRCh38 |
| NC_000019.9:g.1103992C>A , CM000681.1:g.1103992C>A | GRCh37 |
| NC_000019.8:g.1054992C>A | NCBI36 |
| NG_050621.1:g.5068C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706713.1:c.-51C>A | ENSP00000516510.1:n.-51C>A | |
| ENST00000354171.12:c.-51C>A | ENSP00000346103.7:n.-51C>A | |
| ENST00000616066.4:c.-51C>A | ENSP00000485000.1:n.-51C>A | |
| NM_001039847.2:c.-51C>A | NP_001034936.1:n.-51C>A | |
| NM_002085.4:c.-51C>A | NP_002076.2:n.-51C>A |