Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.50196661C= , CM000679.2:g.50196661C= | GRCh38 |
| NC_000017.10:g.48274022C= , CM000679.1:g.48274022C= | GRCh37 |
| NC_000017.9:g.45629021C= | NCBI36 |
| NG_007400.1:g.9979G= , LRG_1:g.9979G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225964.10:c.814G= MANE Select | ENSP00000225964.6:p.Gly272= | |
| ENST00000225964.9:c.814G= | ENSP00000225964.5:p.Gly272= | |
| ENST00000495677.1:n.541G= | ||
| NM_000088.3:c.814G= , LRG_1t1:c.814G= | NP_000079.2:p.Gly272= | |
| XM_005257058.3:c.814G= | XP_005257115.2:p.Gly272= | |
| XM_005257059.3:c.814G= | XP_005257116.2:p.Gly272= | |
| XM_011524341.1:c.814G= | XP_011522643.1:p.Gly272= | |
| XM_005257058.4:c.814G= | XP_005257115.2:p.Gly272= | |
| XM_005257059.4:c.814G= | XP_005257116.2:p.Gly272= | |
| NM_000088.4:c.814G= MANE Select | NP_000079.2:p.Gly272= |