Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67584691G= , CM000673.2:g.67584691G= | GRCh38 |
| NC_000011.9:g.67352162G= , CM000673.1:g.67352162G= | GRCh37 |
| NC_000011.8:g.67108738G= | NCBI36 |
| NG_012075.1:g.6097G= , LRG_723:g.6097G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.151G= | ENSP00000381604.1:p.Gly51= | |
| ENST00000398606.10:c.151G= MANE Select | ENSP00000381607.3:p.Gly51= | |
| ENST00000646888.1:c.44G= | ENSP00000494477.1:p.Arg15= | |
| ENST00000398603.5:c.151G= | ENSP00000381604.1:p.Gly51= | |
| ENST00000398606.7:c.151G= | ENSP00000381607.3:p.Gly51= | |
| ENST00000489040.1:n.150G= | ||
| ENST00000494593.1:n.581G= | ||
| ENST00000498765.5:c.114G= | ||
| NM_000852.3:c.151G= , LRG_723t1:c.151G= | NP_000843.1:p.Gly51= | |
| NM_000852.4:c.151G= MANE Select | NP_000843.1:p.Gly51= |