Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118312086G>A , CM000673.2:g.118312086G>A | GRCh38 |
| NC_000011.9:g.118182801G>A , CM000673.1:g.118182801G>A | GRCh37 |
| NC_000011.8:g.117688011G>A | NCBI36 |
| NG_007383.1:g.12507G>A , LRG_38:g.12507G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000733.4:c.86-67G>A MANE Select | NP_000724.1:n.86-67G>A |
| ENST00000361763.9:c.86-67G>A MANE Select | ENSP00000354566.4:n.86-67G>A |
| NM_000733.3:c.86-67G>A , LRG_38t1:c.86-67G>A | NP_000724.1:n.86-67G>A |
| ENST00000361763.8:c.86-67G>A | ENSP00000354566.4:n.86-67G>A |
| ENST00000526146.5:n.185-67G>A | |
| ENST00000528435.5:n.192-67G>A | |
| ENST00000528600.1:c.86-532G>A | ENSP00000433975.1:n.86-532G>A |
| ENST00000529713.5:n.192-67G>A |