Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55125289T= , CM000666.2:g.55125289T= | GRCh38 |
| NC_000004.11:g.55991456T= , CM000666.1:g.55991456T= | GRCh37 |
| NC_000004.10:g.55686213T= | NCBI36 |
| NG_012004.1:g.5307A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263923.5:c.5A= MANE Select | ENSP00000263923.4:p.Gln2= | |
| ENST00000263923.4:c.5A= | ENSP00000263923.4:p.Gln2= | |
| ENST00000512566.1:n.5A= | ||
| NM_002253.2:c.5A= | NP_002244.1:p.Gln2= | |
| NM_002253.3:c.5A= | NP_002244.1:p.Gln2= | |
| NM_002253.4:c.5A= MANE Select | NP_002244.1:p.Gln2= |