Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189009023G= , CM000664.2:g.189009023G= | GRCh38 |
| NC_000002.11:g.189873749G= , CM000664.1:g.189873749G= | GRCh37 |
| NC_000002.10:g.189581994G= | NCBI36 |
| NG_007404.1:g.39651G= , LRG_3:g.39651G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450867.2:c.3526G= | ENSP00000415346.2:p.Gly1176= | |
| ENST00000304636.9:c.3625G= MANE Select | ENSP00000304408.4:p.Gly1209= | |
| ENST00000304636.7:c.3625G= | ENSP00000304408.3:p.Gly1209= | |
| ENST00000317840.9:c.2716G= | ENSP00000315243.6:p.Gly906= | |
| ENST00000487010.1:n.722G= | ||
| NM_000090.3:c.3625G= , LRG_3t1:c.3625G= | NP_000081.1:p.Gly1209= | |
| NM_000090.4:c.3625G= MANE Select | NP_000081.2:p.Gly1209= |