Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86670978T>A , CM000670.2:g.86670978T>A | GRCh38 |
| NC_000008.10:g.87683206T>A , CM000670.1:g.87683206T>A | GRCh37 |
| NC_000008.9:g.87752322T>A | NCBI36 |
| NG_016980.1:g.77698A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.459A>T MANE Select | ENSP00000316605.5:p.Gly153= | |
| ENST00000680314.1:n.220A>T | ||
| ENST00000681746.1:c.459A>T | ENSP00000505959.1:p.Gly153= | |
| ENST00000320005.5:c.459A>T | ENSP00000316605.5:p.Gly153= | |
| NM_019098.4:c.459A>T | NP_061971.3:p.Gly153= | |
| XM_011517138.1:c.45A>T | XP_011515440.1:p.Gly15= | |
| XM_011517138.2:c.45A>T | XP_011515440.1:p.Gly15= | |
| NM_019098.5:c.459A>T MANE Select | NP_061971.3:p.Gly153= |