Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186192004G= , CM000666.2:g.186192004G= | GRCh38 |
| NC_000004.11:g.187113158G= , CM000666.1:g.187113158G= | GRCh37 |
| NC_000004.10:g.187350152G= | NCBI36 |
| NG_007965.1:g.5485G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_207352.4:c.181G= MANE Select | NP_997235.3:p.Gly61= |
| ENST00000378802.5:c.181G= MANE Select | ENSP00000368079.4:p.Gly61= |
| NM_207352.3:c.181G= | NP_997235.3:p.Gly61= |
| ENST00000378802.4:c.181G= | ENSP00000368079.4:p.Gly61= |
| XM_005262935.2:c.181G= | XP_005262992.1:p.Gly61= |
| XM_005262935.4:c.181G= | XP_005262992.1:p.Gly61= |
| XM_017008037.1:c.-130G= | XP_016863526.1:n.-130G= |