Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.3225653C>A , CM000668.2:g.3225653C>A | GRCh38 |
| NC_000006.11:g.3225887C>A , CM000668.1:g.3225887C>A | GRCh37 |
| NC_000006.10:g.3170886C>A | NCBI36 |
| NG_016715.1:g.7082G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259818.8:c.436G>T MANE Select | ENSP00000259818.6:p.Gly146Trp | |
| ENST00000680070.1:n.1366G>T | ||
| ENST00000681707.1:n.1263G>T | ||
| ENST00000681757.1:n.741G>T | ||
| ENST00000259818.7:c.436G>T | ENSP00000259818.6:p.Gly146Trp | |
| ENST00000473006.1:n.553G>T | ||
| NM_178012.4:c.436G>T | NP_821080.1:p.Gly146Trp | |
| XM_011514571.1:c.220G>T | XP_011512873.1:p.Gly74Trp | |
| NM_178012.5:c.436G>T MANE Select | NP_821080.1:p.Gly146Trp |