Linked Data
gnomAD v4:
16-177413-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.177413C>T , CM000678.2:g.177413C>T | GRCh38 |
| NC_000016.9:g.227412C>T , CM000678.1:g.227412C>T | GRCh37 |
| NC_000016.8:g.167412C>T | NCBI36 |
| NG_000006.1:g.38276C>T | |
| NG_059186.1:g.5763C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000320868.9:c.*2C>T MANE Select | ENSP00000322421.5:n.*2C>T | |
| ENST00000397797.1:c.*2C>T | ENSP00000380899.1:n.*2C>T | |
| ENST00000472694.1:n.567C>T | ||
| NM_000558.4:c.*2C>T | NP_000549.1:n.*2C>T | |
| NM_000558.5:c.*2C>T MANE Select | NP_000549.1:n.*2C>T |