Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.50195934C= , CM000679.2:g.50195934C= | GRCh38 |
| NC_000017.10:g.48273295C= , CM000679.1:g.48273295C= | GRCh37 |
| NC_000017.9:g.45628294C= | NCBI36 |
| NG_007400.1:g.10706G= , LRG_1:g.10706G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225964.10:c.1045G= MANE Select | ENSP00000225964.6:p.Val349= | |
| ENST00000225964.9:c.1045G= | ENSP00000225964.5:p.Val349= | |
| NM_000088.3:c.1045G= , LRG_1t1:c.1045G= | NP_000079.2:p.Val349= | |
| XM_005257058.3:c.1045G= | XP_005257115.2:p.Val349= | |
| XM_005257059.3:c.957+380G= | XP_005257116.2:n.957+380G= | |
| XM_011524341.1:c.957+380G= | XP_011522643.1:n.957+380G= | |
| XM_005257058.4:c.1045G= | XP_005257115.2:p.Val349= | |
| XM_005257059.4:c.957+380G= | XP_005257116.2:n.957+380G= | |
| NM_000088.4:c.1045G= MANE Select | NP_000079.2:p.Val349= |