Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52038228T= , CM000666.2:g.52038228T= | GRCh38 |
| NC_000004.11:g.52904394T= , CM000666.1:g.52904394T= | GRCh37 |
| NC_000004.10:g.52599151T= | NCBI36 |
| NG_008891.1:g.5092A= , LRG_204:g.5092A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000232.5:c.32A= MANE Select | NP_000223.1:p.Gln11= |
| ENST00000381431.10:c.32A= MANE Select | ENSP00000370839.6:p.Gln11= |
| NM_000232.4:c.32A= , LRG_204t1:c.32A= | NP_000223.1:p.Gln11= |
| ENST00000381431.9:c.32A= | ENSP00000370839.5:p.Gln11= |
| ENST00000506357.5:c.18A= | |
| XM_011534403.1:c.32A= | XP_011532705.1:p.Gln11= |