Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48476822G= , CM000675.2:g.48476822G= | GRCh38 |
| NC_000013.10:g.49050958G= , CM000675.1:g.49050958G= | GRCh37 |
| NC_000013.9:g.47948959G= | NCBI36 |
| NG_009009.1:g.178076G= , LRG_517:g.178076G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.2642G= MANE Select | ENSP00000267163.4:p.Gly881= | |
| ENST00000643064.1:c.194+95379G= | ||
| ENST00000650461.1:c.2642G= | ENSP00000497193.1:p.Gly881= | |
| ENST00000267163.4:c.2642G= | ENSP00000267163.4:p.Gly881= | |
| ENST00000484879.1:n.376G= | ||
| ENST00000531171.5:n.245G= | ||
| NM_000321.2:c.2642G= , LRG_517t1:c.2642G= | NP_000312.2:p.Gly881= | |
| XM_011535171.1:c.2381G= | XP_011533473.1:p.Gly794= | |
| XM_011535171.2:c.2381G= | XP_011533473.1:p.Gly794= | |
| NM_000321.3:c.2642G= MANE Select | NP_000312.2:p.Gly881= |