Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.50192946A>C , CM000685.2:g.50192946A>C | GRCh38 |
| NC_000023.10:g.49957597A>C , CM000685.1:g.49957597A>C | GRCh37 |
| NC_000023.9:g.49844337A>C | NCBI36 |
| NG_012552.1:g.13068T>G | |
| NG_012552.2:g.13068T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358526.7:c.1767T>G MANE Select | ENSP00000351327.2:p.Gly589= | |
| ENST00000358526.6:c.1767T>G | ENSP00000351327.2:p.Gly589= | |
| ENST00000376064.7:c.1740T>G | ENSP00000365232.3:p.Gly580= | |
| ENST00000448865.5:c.618T>G | ENSP00000402403.1:p.Gly206= | |
| ENST00000481402.5:n.1879T>G | ||
| NM_003886.2:c.1767T>G | NP_003877.2:p.Gly589= | |
| NM_139289.1:c.1740T>G | NP_647450.1:p.Gly580= | |
| NM_003886.3:c.1767T>G MANE Select | NP_003877.2:p.Gly589= | |
| NM_139289.2:c.1740T>G | NP_647450.1:p.Gly580= |