Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24145889A>G , CM000668.2:g.24145889A>G | GRCh38 |
| NC_000006.11:g.24146117A>G , CM000668.1:g.24146117A>G | GRCh37 |
| NC_000006.10:g.24254096A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378491.9:c.531A>G MANE Select | ENSP00000367752.4:p.Thr177= | |
| ENST00000378478.5:c.531A>G | ENSP00000367739.2:p.Thr177= | |
| ENST00000378491.8:c.531A>G | ENSP00000367752.4:p.Thr177= | |
| ENST00000468195.2:n.257-8882A>G | ||
| NM_080723.4:c.531A>G | NP_542454.3:p.Thr177= | |
| NM_080723.5:c.531A>G MANE Select | NP_542454.3:p.Thr177= |