Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.196996127A>G , CM000663.2:g.196996127A>G | GRCh38 |
| NC_000001.10:g.196965257A>G , CM000663.1:g.196965257A>G | GRCh37 |
| NC_000001.9:g.195231880A>G | NCBI36 |
| NG_016365.1:g.23591A>G , LRG_227:g.23591A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699466.1:c.641A>G | ENSP00000514393.1:p.Asn214Ser | |
| ENST00000699467.1:n.965A>G | ||
| ENST00000699468.1:c.-11A>G | ENSP00000514394.1:n.-11A>G | |
| ENST00000256785.5:c.896A>G MANE Select | ENSP00000256785.4:p.Asn299Ser | |
| ENST00000256785.4:c.896A>G | ENSP00000256785.4:p.Asn299Ser | |
| NM_030787.3:c.896A>G , LRG_227t1:c.896A>G | NP_110414.1:p.Asn299Ser | |
| XM_011510020.1:c.905A>G | XP_011508322.1:p.Asn302Ser | |
| XM_011510020.2:c.905A>G | XP_011508322.1:p.Asn302Ser | |
| NM_030787.4:c.896A>G MANE Select | NP_110414.1:p.Asn299Ser |