Linked Data
gnomAD v4:
X-68829768-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.68829768C>A , CM000685.2:g.68829768C>A | GRCh38 |
| NC_000023.10:g.68049611C>A , CM000685.1:g.68049611C>A | GRCh37 |
| NC_000023.9:g.67966336C>A | NCBI36 |
| NG_008887.1:g.5772C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000204961.5:c.-9C>A MANE Select | ENSP00000204961.4:n.-9C>A | |
| ENST00000204961.4:c.-9C>A | ENSP00000204961.4:n.-9C>A | |
| NM_004429.4:c.-9C>A | NP_004420.1:n.-9C>A | |
| NM_004429.5:c.-9C>A MANE Select | NP_004420.1:n.-9C>A |