Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.88008175G= , CM000666.2:g.88008175G= | GRCh38 |
| NC_000004.11:g.88929327G= , CM000666.1:g.88929327G= | GRCh37 |
| NC_000004.10:g.89148351G= | NCBI36 |
| NG_008604.1:g.5508G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000237596.7:c.442G= MANE Select | ENSP00000237596.2:p.Gly148= | |
| ENST00000237596.6:c.442G= | ENSP00000237596.2:p.Gly148= | |
| NM_000297.3:c.442G= | NP_000288.1:p.Gly148= | |
| XM_011532028.1:c.442G= | XP_011530330.1:p.Gly148= | |
| XR_244632.2:n.537G= | ||
| NR_156488.1:n.529G= | ||
| XM_011532028.2:c.442G= | XP_011530330.1:p.Gly148= | |
| NM_000297.4:c.442G= MANE Select | NP_000288.1:p.Gly148= | |
| NR_156488.2:n.541G= |