Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.216323585A>G , CM000663.2:g.216323585A>G | GRCh38 |
| NC_000001.10:g.216496927A>G , CM000663.1:g.216496927A>G | GRCh37 |
| NC_000001.9:g.214563550A>G | NCBI36 |
| NG_009497.1:g.104812T>C | |
| NG_009497.2:g.104864T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_206933.4:c.1439T>C MANE Select | NP_996816.3:p.Val480Ala |
| ENST00000307340.8:c.1439T>C MANE Select | ENSP00000305941.3:p.Val480Ala |
| NM_007123.5:c.1439T>C | NP_009054.5:p.Val480Ala |
| NM_007123.6:c.1439T>C | NP_009054.6:p.Val480Ala |
| NM_206933.2:c.1439T>C | NP_996816.2:p.Val480Ala |
| NM_206933.3:c.1439T>C | NP_996816.2:p.Val480Ala |
| ENST00000307340.7:c.1439T>C | ENSP00000305941.3:p.Val480Ala |
| ENST00000366942.3:c.1439T>C | ENSP00000355909.3:p.Val480Ala |
| ENST00000674083.1:c.1439T>C | ENSP00000501296.1:p.Val480Ala |