Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.162318034C= , CM000664.2:g.162318034C= | GRCh38 |
| NC_000002.11:g.163174544C= , CM000664.1:g.163174544C= | GRCh37 |
| NC_000002.10:g.162882790C= | NCBI36 |
| NG_011495.1:g.5496G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_022168.4:c.274G= MANE Select | NP_071451.2:p.Ala92= |
| ENST00000649979.2:c.274G= MANE Select | ENSP00000497271.1:p.Ala92= |
| NM_022168.3:c.274G= | NP_071451.2:p.Ala92= |
| ENST00000263642.2:c.274G= | ENSP00000263642.2:p.Ala92= |
| ENST00000421365.2:c.274G= | ENSP00000408450.2:p.Ala92= |
| ENST00000648433.1:c.274G= | ENSP00000496816.1:p.Ala92= |
| ENST00000679938.1:c.109G= | ENSP00000505518.1:p.Ala37= |
| ENST00000697291.1:c.274G= | ENSP00000513228.1:p.Ala92= |
| XM_011511629.1:c.274G= | XP_011509931.1:p.Ala92= |