Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.196996128T= , CM000663.2:g.196996128T= | GRCh38 |
| NC_000001.10:g.196965258T= , CM000663.1:g.196965258T= | GRCh37 |
| NC_000001.9:g.195231881T= | NCBI36 |
| NG_016365.1:g.23592T= , LRG_227:g.23592T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699466.1:c.642T= | ENSP00000514393.1:p.Asn214= | |
| ENST00000699467.1:n.966T= | ||
| ENST00000699468.1:c.-10T= | ENSP00000514394.1:n.-10T= | |
| ENST00000256785.5:c.897T= MANE Select | ENSP00000256785.4:p.Asn299= | |
| ENST00000256785.4:c.897T= | ENSP00000256785.4:p.Asn299= | |
| NM_030787.3:c.897T= , LRG_227t1:c.897T= | NP_110414.1:p.Asn299= | |
| XM_011510020.1:c.906T= | XP_011508322.1:p.Asn302= | |
| XM_011510020.2:c.906T= | XP_011508322.1:p.Asn302= | |
| NM_030787.4:c.897T= MANE Select | NP_110414.1:p.Asn299= |