Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.118110245C= , CM000670.2:g.118110245C= | GRCh38 |
| NC_000008.10:g.119122484C= , CM000670.1:g.119122484C= | GRCh37 |
| NC_000008.9:g.119191665C= | NCBI36 |
| NG_007455.2:g.6575G= , LRG_493:g.6575G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378204.7:c.802G= MANE Select | ENSP00000367446.3:p.Gly268= | |
| ENST00000436216.2:c.170G= | ||
| ENST00000378204.6:c.802G= | ENSP00000367446.2:p.Gly268= | |
| ENST00000436216.1:c.170G= | ||
| ENST00000437196.1:c.73+729G= | ENSP00000407299.1:n.73+729G= | |
| NM_000127.2:c.802G= , LRG_493t1:c.802G= | NP_000118.2:p.Gly268= | |
| NM_000127.3:c.802G= MANE Select | NP_000118.2:p.Gly268= |