Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.70672562G>T , CM000676.2:g.70672562G>T | GRCh38 |
| NC_000014.8:g.71139279G>T , CM000676.1:g.71139279G>T | GRCh37 |
| NC_000014.7:g.70209032G>T | NCBI36 |
| NG_012648.1:g.35776G>T | |
| NG_012648.2:g.35776G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256367.3:c.*1407G>T MANE Select | ENSP00000256367.2:n.*1407G>T | |
| ENST00000256367.2:c.*1407G>T | ENSP00000256367.2:n.*1407G>T | |
| NM_015351.1:c.*1407G>T | NP_056166.1:n.*1407G>T | |
| NM_015351.2:c.*1407G>T MANE Select | NP_056166.1:n.*1407G>T |