Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.100277461A>G , CM000676.2:g.100277461A>G | GRCh38 |
| NC_000014.8:g.100743798A>G , CM000676.1:g.100743798A>G | GRCh37 |
| NC_000014.7:g.99813551A>G | NCBI36 |
| NG_046908.1:g.43697A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003403.5:c.1106A>G MANE Select | NP_003394.1:p.Asn369Ser |
| ENST00000262238.10:c.1106A>G MANE Select | ENSP00000262238.4:p.Asn369Ser |
| NM_003403.4:c.1106A>G | NP_003394.1:p.Asn369Ser |
| ENST00000262238.8:c.1106A>G | ENSP00000262238.4:p.Asn369Ser |
| ENST00000554579.1:n.494A>G | |
| ENST00000554804.1:c.433A>G | |
| ENST00000623799.1:n.1733A>G | |
| ENST00000651219.1:c.596A>G | ENSP00000498329.1:n.596A>G |
| ENST00000704024.1:n.1155A>G | |
| ENST00000704485.1:c.344A>G | ENSP00000515913.1:p.Asn115Ser |