Linked Data
gnomAD v4:
10-94989177-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94989177C>T , CM000672.2:g.94989177C>T | GRCh38 |
| NC_000010.10:g.96748934C>T , CM000672.1:g.96748934C>T | GRCh37 |
| NC_000010.9:g.96738924C>T | NCBI36 |
| NG_008385.1:g.55520C>T | |
| NG_008385.2:g.56020C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.*149C>T MANE Select | ENSP00000260682.6:n.*149C>T | |
| ENST00000643112.1:c.*631C>T | ENSP00000496202.1:n.*631C>T | |
| ENST00000260682.6:c.*149C>T | ENSP00000260682.6:n.*149C>T | |
| NM_000771.3:c.*149C>T | NP_000762.2:n.*149C>T | |
| NM_000771.4:c.*149C>T MANE Select | NP_000762.2:n.*149C>T |