Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.6097013C>T , CM000682.2:g.6097013C>T | GRCh38 |
| NC_000020.10:g.6077660C>T , CM000682.1:g.6077660C>T | GRCh37 |
| NC_000020.9:g.6025660C>T | NCBI36 |
| NG_016213.1:g.31532G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_017671.5:c.978G>A MANE Select | NP_060141.3:p.Ser326= |
| ENST00000217289.9:c.978G>A MANE Select | ENSP00000217289.4:p.Ser326= |
| NM_017671.4:c.978G>A | NP_060141.3:p.Ser326= |
| ENST00000217289.8:c.978G>A | ENSP00000217289.4:p.Ser326= |
| ENST00000536936.1:c.207G>A | ENSP00000441063.1:p.Ser69= |
| ENST00000699095.1:c.978G>A | ENSP00000514127.1:p.Ser326= |
| ENST00000699096.1:n.1440G>A | |
| ENST00000699097.1:n.148G>A | |
| XM_024451935.1:c.978G>A | XP_024307703.1:p.Ser326= |