Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52675442T>C , CM000674.2:g.52675442T>C | GRCh38 |
| NC_000012.11:g.53069226T>C , CM000674.1:g.53069226T>C | GRCh37 |
| NC_000012.10:g.51355493T>C | NCBI36 |
| NG_008364.1:g.9966A>G | |
| NG_008364.2:g.9966A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252244.3:c.1686A>G MANE Select | ENSP00000252244.3:p.Gly562= | |
| NM_006121.3:c.1686A>G | NP_006112.3:p.Gly562= | |
| NM_006121.4:c.1686A>G MANE Select | NP_006112.3:p.Gly562= |