Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6034727T>C , CM000674.2:g.6034727T>C | GRCh38 |
| NC_000012.11:g.6143893T>C , CM000674.1:g.6143893T>C | GRCh37 |
| NC_000012.10:g.6014154T>C | NCBI36 |
| NG_009072.1:g.94944A>G | |
| NG_009072.2:g.94944A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261405.10:c.2646A>G MANE Select | ENSP00000261405.5:p.Lys882= | |
| ENST00000261405.9:c.2646A>G | ENSP00000261405.5:p.Lys882= | |
| ENST00000538635.5:n.421-40793A>G | ||
| NM_000552.3:c.2646A>G | NP_000543.2:p.Lys882= | |
| NM_000552.4:c.2646A>G | NP_000543.2:p.Lys882= | |
| NM_000552.5:c.2646A>G MANE Select | NP_000543.3:p.Lys882= |