Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128254252G= , CM000669.2:g.128254252G= | GRCh38 |
| NC_000007.13:g.127894305G= , CM000669.1:g.127894305G= | GRCh37 |
| NC_000007.12:g.127681541G= | NCBI36 |
| NG_007450.1:g.17975G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000230.3:c.145-152G= MANE Select | NP_000221.1:n.145-152G= |
| ENST00000308868.5:c.145-152G= MANE Select | ENSP00000312652.4:n.145-152G= |
| NM_000230.2:c.145-152G= | NP_000221.1:n.145-152G= |
| ENST00000308868.4:c.145-152G= | ENSP00000312652.4:n.145-152G= |
| XM_005250340.3:c.145-155G= | XP_005250397.1:n.145-155G= |
| XM_005250340.5:c.145-155G= | XP_005250397.1:n.145-155G= |