Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44287005G= , CM000683.2:g.44287005G= | GRCh38 |
| NC_000021.8:g.45706888G= , CM000683.1:g.45706888G= | GRCh37 |
| NC_000021.7:g.44531316G= | NCBI36 |
| NG_009556.1:g.6126G= , LRG_18:g.6126G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291582.6:c.335G= MANE Select | ENSP00000291582.5:p.Gly112= | |
| ENST00000291582.5:c.335G= | ENSP00000291582.5:p.Gly112= | |
| ENST00000527919.5:n.496G= | ||
| ENST00000530812.5:n.504G= | ||
| NM_000383.3:c.335G= | NP_000374.1:p.Gly112= | |
| XM_011529551.1:c.335G= | XP_011527853.1:p.Gly112= | |
| NM_000383.4:c.335G= MANE Select | NP_000374.1:p.Gly112= |