Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94415245G= , CM000669.2:g.94415245G= | GRCh38 |
| NC_000007.13:g.94044557G= , CM000669.1:g.94044557G= | GRCh37 |
| NC_000007.12:g.93882493G= | NCBI36 |
| NG_007405.1:g.25685G= , LRG_2:g.25685G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000089.4:c.1739G= MANE Select | NP_000080.2:p.Gly580= |
| ENST00000297268.11:c.1739G= MANE Select | ENSP00000297268.6:p.Gly580= |
| NM_000089.3:c.1739G= , LRG_2t1:c.1739G= | NP_000080.2:p.Gly580= |
| ENST00000297268.10:c.1739G= | ENSP00000297268.6:p.Gly580= |
| ENST00000473573.5:n.76G= | |
| ENST00000488298.5:n.163G= | |
| ENST00000620463.1:c.1733G= | ENSP00000477719.1:p.Gly578= |