Linked Data
gnomAD v4:
X-25004481-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25004481C>T , CM000685.2:g.25004481C>T | GRCh38 |
| NC_000023.10:g.25022598C>T , CM000685.1:g.25022598C>T | GRCh37 |
| NC_000023.9:g.24932519C>T | NCBI36 |
| NG_008281.1:g.16468G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379044.5:c.*189G>A MANE Select | ENSP00000368332.4:n.*189G>A | |
| ENST00000379044.4:c.*189G>A | ENSP00000368332.4:n.*189G>A | |
| NM_139058.2:c.*189G>A | NP_620689.1:n.*189G>A | |
| NM_139058.3:c.*189G>A MANE Select | NP_620689.1:n.*189G>A |