Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154158844G= , CM000685.2:g.154158844G= | GRCh38 |
| NC_000023.10:g.153424319G= , CM000685.1:g.153424319G= | GRCh37 |
| NC_000023.9:g.153077513G= | NCBI36 |
| NG_009105.2:g.19594G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369951.9:c.1013G= MANE Select | ENSP00000358967.4:p.Gly338= | |
| ENST00000369951.8:c.1013G= | ENSP00000358967.4:p.Gly338= | |
| ENST00000442922.1:c.413G= | ENSP00000402493.1:p.Gly138= | |
| NM_020061.5:c.1013G= | NP_064445.2:p.Gly338= | |
| NM_020061.6:c.1013G= MANE Select | NP_064445.2:p.Gly338= |