Linked Data
gnomAD v4:
10-94941689-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94941689A>T , CM000672.2:g.94941689A>T | GRCh38 |
| NC_000010.10:g.96701446A>T , CM000672.1:g.96701446A>T | GRCh37 |
| NC_000010.9:g.96691436A>T | NCBI36 |
| NG_008385.1:g.8032A>T | |
| NG_008385.2:g.8532A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.169-169A>T MANE Select | ENSP00000260682.6:n.169-169A>T | |
| ENST00000643112.1:c.169-169A>T | ENSP00000496202.1:n.169-169A>T | |
| ENST00000645207.1:n.153A>T | ||
| ENST00000260682.6:c.169-169A>T | ENSP00000260682.6:n.169-169A>T | |
| ENST00000461906.1:n.194-169A>T | ||
| NM_000771.3:c.169-169A>T | NP_000762.2:n.169-169A>T | |
| NM_000771.4:c.169-169A>T MANE Select | NP_000762.2:n.169-169A>T |