Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.101348551C= , CM000685.2:g.101348551C= | GRCh38 |
| NC_000023.10:g.100603539C= , CM000685.1:g.100603539C= | GRCh37 |
| NC_000023.9:g.100490195C= | NCBI36 |
| NG_009616.1:g.42674G= , LRG_128:g.42674G= | |
| NG_011734.1:g.5419G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372902.4:c.114G= MANE Select | ENSP00000361993.3:p.Gln38= | |
| ENST00000644112.2:c.114G= | ENSP00000494385.1:p.Gln38= | |
| ENST00000645279.1:c.114G= | ENSP00000494239.1:p.Gln38= | |
| ENST00000647480.1:n.25G= | ||
| ENST00000372902.3:c.114G= | ENSP00000361993.3:p.Gln38= | |
| ENST00000480575.1:n.199G= | ||
| NM_001145951.1:c.114G= | NP_001139423.1:p.Gln38= | |
| NM_004085.3:c.114G= | NP_004076.1:p.Gln38= | |
| NM_004085.4:c.114G= MANE Select | NP_004076.1:p.Gln38= | |
| NM_001145951.2:c.114G= | NP_001139423.1:p.Gln38= |