Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111106140G= , CM000667.2:g.111106140G= | GRCh38 |
| NC_000005.9:g.110441839G= , CM000667.1:g.110441839G= | GRCh37 |
| NC_000005.8:g.110469738G= | NCBI36 |
| NG_008979.1:g.18970G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000513710.4:c.1177G= MANE Select | ENSP00000424628.3:p.Ala393= | |
| ENST00000505303.5:n.1313G= | ||
| ENST00000506538.6:c.1345G= | ENSP00000423067.2:p.Ala449= | |
| ENST00000513710.3:c.1177G= | ENSP00000424628.3:p.Ala393= | |
| ENST00000612402.4:c.1345G= | ENSP00000479950.1:p.Ala449= | |
| NM_139281.2:c.1345G= | NP_644810.1:p.Ala449= | |
| XM_011543163.1:c.1345G= | XP_011541465.1:p.Ala449= | |
| NM_139281.3:c.1177G= MANE Select | NP_644810.2:p.Ala393= |