Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44292273A= , CM000683.2:g.44292273A= | GRCh38 |
| NC_000021.8:g.45712156A= , CM000683.1:g.45712156A= | GRCh37 |
| NC_000021.7:g.44536584A= | NCBI36 |
| NG_009556.1:g.11394A= , LRG_18:g.11394A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291582.6:c.996-29A= MANE Select | ENSP00000291582.5:n.996-29A= | |
| ENST00000291582.5:c.996-29A= | ENSP00000291582.5:n.996-29A= | |
| ENST00000337909.5:n.457-29A= | ||
| ENST00000397994.8:n.457-29A= | ||
| ENST00000527919.5:n.1726-29A= | ||
| ENST00000530812.5:n.2743-29A= | ||
| NM_000383.3:c.996-29A= | NP_000374.1:n.996-29A= | |
| XM_011529551.1:c.993-29A= | XP_011527853.1:n.993-29A= | |
| NM_000383.4:c.996-29A= MANE Select | NP_000374.1:n.996-29A= |