Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6529949T>G , CM000674.2:g.6529949T>G | GRCh38 |
| NC_000012.11:g.6639115T>G , CM000674.1:g.6639115T>G | GRCh37 |
| NC_000012.10:g.6509376T>G | NCBI36 |
| NG_007073.2:g.459T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_014865.4:c.3828T>G MANE Select | NP_055680.3:p.Pro1276= |
| ENST00000315579.10:c.3828T>G MANE Select | ENSP00000325017.5:p.Pro1276= |
| NM_014865.3:c.3828T>G | NP_055680.3:p.Pro1276= |
| ENST00000315579.9:c.3828T>G | ENSP00000325017.5:p.Pro1276= |
| ENST00000539084.5:c.*3523T>G | ENSP00000438495.1:n.*3523T>G |
| ENST00000539885.1:n.509T>G |