Linked Data
gnomAD v4:
11-72243826-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.72243826C>A , CM000673.2:g.72243826C>A | GRCh38 |
| NC_000011.9:g.71954870C>A , CM000673.1:g.71954870C>A | GRCh37 |
| NC_000011.8:g.71632518C>A | NCBI36 |
| NG_008169.1:g.5351G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000298231.5:c.179G>T MANE Select | ENSP00000298231.5:p.Gly60Val | |
| ENST00000544057.1:n.85+1754G>T | ||
| NM_005169.3:c.179G>T | NP_005160.2:p.Gly60Val | |
| NM_005169.4:c.179G>T MANE Select | NP_005160.2:p.Gly60Val |