Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48367521G= , CM000675.2:g.48367521G= | GRCh38 |
| NC_000013.10:g.48941657G= , CM000675.1:g.48941657G= | GRCh37 |
| NC_000013.9:g.47839658G= | NCBI36 |
| NG_009009.1:g.68775G= , LRG_517:g.68775G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000321.3:c.967G= MANE Select | NP_000312.2:p.Glu323= |
| ENST00000267163.6:c.967G= MANE Select | ENSP00000267163.4:p.Glu323= |
| NM_000321.2:c.967G= , LRG_517t1:c.967G= | NP_000312.2:p.Glu323= |
| ENST00000267163.4:c.967G= | ENSP00000267163.4:p.Glu323= |
| ENST00000650461.1:c.967G= | ENSP00000497193.1:p.Glu323= |
| XM_011535171.1:c.706G= | XP_011533473.1:p.Glu236= |
| XM_011535171.2:c.706G= | XP_011533473.1:p.Glu236= |
| XR_002957522.1:n.122-2545C= |