Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.100276648G>A , CM000676.2:g.100276648G>A | GRCh38 |
| NC_000014.8:g.100742985G>A , CM000676.1:g.100742985G>A | GRCh37 |
| NC_000014.7:g.99812738G>A | NCBI36 |
| NG_046908.1:g.42884G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003403.5:c.1062G>A MANE Select | NP_003394.1:p.Gln354= |
| ENST00000262238.10:c.1062G>A MANE Select | ENSP00000262238.4:p.Gln354= |
| NM_003403.4:c.1062G>A | NP_003394.1:p.Gln354= |
| ENST00000262238.8:c.1062G>A | ENSP00000262238.4:p.Gln354= |
| ENST00000554579.1:n.450G>A | |
| ENST00000554804.1:c.390-770G>A | |
| ENST00000623799.1:n.920G>A | |
| ENST00000651219.1:c.552G>A | ENSP00000498329.1:n.552G>A |
| ENST00000704024.1:n.1111G>A | |
| ENST00000704485.1:c.300G>A | ENSP00000515913.1:p.Gln100= |