Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29072996A= , CM000664.2:g.29072996A= | GRCh38 |
| NC_000002.11:g.29295862A= , CM000664.1:g.29295862A= | GRCh37 |
| NC_000002.10:g.29149366A= | NCBI36 |
| NG_021427.1:g.6266T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331664.6:c.1266T= MANE Select | ENSP00000332809.4:p.Val422= | |
| ENST00000331664.5:c.1266T= | ENSP00000332809.4:p.Val422= | |
| NM_001029883.2:c.1266T= | NP_001025054.1:p.Val422= | |
| XM_011532826.1:c.1266T= | XP_011531128.1:p.Val422= | |
| XR_939901.1:n.185+3829A= | ||
| XR_939902.1:n.173+3841A= | ||
| NM_001029883.3:c.1266T= MANE Select | NP_001025054.1:p.Val422= |