Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.216201914G>T , CM000664.2:g.216201914G>T | GRCh38 |
| NC_000002.11:g.217066637G>T , CM000664.1:g.217066637G>T | GRCh37 |
| NC_000002.10:g.216774882G>T | NCBI36 |
| NG_029780.1:g.97618G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392132.7:c.2110-2408G>T MANE Select | ENSP00000375977.2:n.2110-2408G>T | |
| ENST00000392132.6:c.2110-2408G>T | ENSP00000375977.2:n.2110-2408G>T | |
| ENST00000392133.7:c.2110-2408G>T | ENSP00000375978.3:n.2110-2408G>T | |
| ENST00000460284.5:n.2652-2408G>T | ||
| NM_021141.3:c.2110-2408G>T | NP_066964.1:n.2110-2408G>T | |
| NM_021141.4:c.2110-2408G>T MANE Select | NP_066964.1:n.2110-2408G>T |