Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.70176268A>G , CM000679.2:g.70176268A>G | GRCh38 |
| NC_000017.10:g.68172409A>G , CM000679.1:g.68172409A>G | GRCh37 |
| NC_000017.9:g.65684004A>G | NCBI36 |
| NG_008798.1:g.11734A>G , LRG_328:g.11734A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000243457.4:c.1229A>G MANE Select | ENSP00000243457.2:p.Asn410Ser | |
| ENST00000243457.3:c.1229A>G | ENSP00000243457.2:p.Asn410Ser | |
| ENST00000535240.1:c.1229A>G | ENSP00000441848.1:p.Asn410Ser | |
| NM_000891.2:c.1229A>G , LRG_328t1:c.1229A>G | NP_000882.1:p.Asn410Ser | |
| XM_011524779.1:c.1229A>G | XP_011523081.1:p.Asn410Ser | |
| NM_000891.3:c.1229A>G MANE Select | NP_000882.1:p.Asn410Ser |