Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.25123996C= , CM000669.2:g.25123996C= | GRCh38 |
| NC_000007.13:g.25163615C= , CM000669.1:g.25163615C= | GRCh37 |
| NC_000007.12:g.25130140C= | NCBI36 |
| NG_023438.1:g.6366G= , LRG_876:g.6366G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_018947.6:c.124G= MANE Select | NP_061820.1:p.Gly42= |
| ENST00000305786.7:c.124G= MANE Select | ENSP00000307786.2:p.Gly42= |
| NM_018947.5:c.124G= , LRG_876t1:c.124G= | NP_061820.1:p.Gly42= |
| ENST00000305786.6:c.124G= | ENSP00000307786.2:p.Gly42= |
| ENST00000409409.5:c.124G= | ENSP00000386270.1:p.Gly42= |
| ENST00000409764.5:c.124G= | ENSP00000387279.1:p.Gly42= |
| ENST00000413447.1:c.124G= | ENSP00000416479.1:p.Gly42= |