Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111106140G>T , CM000667.2:g.111106140G>T | GRCh38 |
| NC_000005.9:g.110441839G>T , CM000667.1:g.110441839G>T | GRCh37 |
| NC_000005.8:g.110469738G>T | NCBI36 |
| NG_008979.1:g.18970G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_139281.3:c.1177G>T MANE Select | NP_644810.2:p.Ala393Ser |
| ENST00000513710.4:c.1177G>T MANE Select | ENSP00000424628.3:p.Ala393Ser |
| NM_139281.2:c.1345G>T | NP_644810.1:p.Ala449Ser |
| ENST00000505303.5:n.1313G>T | |
| ENST00000506538.6:c.1345G>T | ENSP00000423067.2:p.Ala449Ser |
| ENST00000513710.3:c.1177G>T | ENSP00000424628.3:p.Ala393Ser |
| ENST00000612402.4:c.1345G>T | ENSP00000479950.1:p.Ala449Ser |
| XM_011543163.1:c.1345G>T | XP_011541465.1:p.Ala449Ser |