Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.99845627G= , CM000672.2:g.99845627G= | GRCh38 |
| NC_000010.10:g.101605384G= , CM000672.1:g.101605384G= | GRCh37 |
| NC_000010.9:g.101595374G= | NCBI36 |
| NG_011798.1:g.67922G= | |
| NG_011798.2:g.68030G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647814.1:c.3991G= MANE Select | ENSP00000497274.1:p.Gly1331= | |
| ENST00000649459.1:n.339G= | ||
| ENST00000370449.8:c.3991G= | ENSP00000359478.4:p.Gly1331= | |
| NM_000392.4:c.3991G= | NP_000383.1:p.Gly1331= | |
| XM_006717630.2:c.3295G= | XP_006717693.1:p.Gly1099= | |
| XR_945604.1:n.4177-56G= | ||
| XR_945605.1:n.4055G= | ||
| NM_000392.5:c.3991G= MANE Select | NP_000383.2:p.Gly1331= | |
| XM_006717630.3:c.3295G= | XP_006717693.1:p.Gly1099= | |
| XR_945604.3:n.4231-56G= | ||
| XR_945605.3:n.4107G= |