Linked Data
gnomAD v4:
10-92637472-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.92637472C>T , CM000672.2:g.92637472C>T | GRCh38 |
| NC_000010.10:g.94397229C>T , CM000672.1:g.94397229C>T | GRCh37 |
| NC_000010.9:g.94387209C>T | NCBI36 |
| NG_032580.1:g.49405C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260731.5:c.2087C>T MANE Select | ENSP00000260731.3:p.Ser696Phe | |
| ENST00000676621.1:c.*605C>T | ENSP00000503639.1:n.*605C>T | |
| ENST00000676647.1:c.1880C>T | ENSP00000503394.1:p.Ser627Phe | |
| ENST00000676757.1:c.1880C>T | ENSP00000504289.1:p.Ser627Phe | |
| ENST00000677720.1:c.*61C>T | ENSP00000504840.1:n.*61C>T | |
| ENST00000260731.4:c.2087C>T | ENSP00000260731.3:p.Ser696Phe | |
| NM_004523.3:c.2087C>T | NP_004514.2:p.Ser696Phe | |
| NM_004523.4:c.2087C>T MANE Select | NP_004514.2:p.Ser696Phe |