Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94414242T>A , CM000669.2:g.94414242T>A | GRCh38 |
| NC_000007.13:g.94043554T>A , CM000669.1:g.94043554T>A | GRCh37 |
| NC_000007.12:g.93881490T>A | NCBI36 |
| NG_007405.1:g.24682T>A , LRG_2:g.24682T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000089.4:c.1686T>A MANE Select | NP_000080.2:p.Gly562= |
| ENST00000297268.11:c.1686T>A MANE Select | ENSP00000297268.6:p.Gly562= |
| NM_000089.3:c.1686T>A , LRG_2t1:c.1686T>A | NP_000080.2:p.Gly562= |
| ENST00000297268.10:c.1686T>A | ENSP00000297268.6:p.Gly562= |
| ENST00000473573.5:n.23T>A | |
| ENST00000488298.5:n.110T>A | |
| ENST00000620463.1:c.1680T>A | ENSP00000477719.1:p.Gly560= |