Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110601820T>C , CM000672.2:g.110601820T>C | GRCh38 |
| NC_000010.10:g.112361578T>C , CM000672.1:g.112361578T>C | GRCh37 |
| NC_000010.9:g.112351568T>C | NCBI36 |
| NG_012217.1:g.39130T>C , LRG_774:g.39130T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.5061T>C | ||
| ENST00000685743.1:n.2536T>C | ||
| ENST00000686057.1:n.1179T>C | ||
| ENST00000689321.1:n.1791T>C | ||
| ENST00000689986.1:n.617T>C | ||
| ENST00000361804.5:c.2828T>C MANE Select | ENSP00000354720.5:p.Ile943Thr | |
| ENST00000361804.4:c.2828T>C | ENSP00000354720.4:p.Ile943Thr | |
| NM_005445.3:c.2828T>C , LRG_774t1:c.2828T>C | NP_005436.1:p.Ile943Thr | |
| NM_005445.4:c.2828T>C MANE Select | NP_005436.1:p.Ile943Thr |