Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128305547C>T , CM000667.2:g.128305547C>T | GRCh38 |
| NC_000005.9:g.127641239C>T , CM000667.1:g.127641239C>T | GRCh37 |
| NC_000005.8:g.127669138C>T | NCBI36 |
| NG_008750.1:g.237497G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001999.4:c.5638G>A MANE Select | NP_001990.2:p.Ala1880Thr |
| ENST00000262464.9:c.5638G>A MANE Select | ENSP00000262464.4:p.Ala1880Thr |
| NM_001999.3:c.5638G>A | NP_001990.2:p.Ala1880Thr |
| ENST00000262464.8:c.5638G>A | ENSP00000262464.4:p.Ala1880Thr |
| ENST00000508053.5:c.5638G>A | ENSP00000424571.1:p.Ala1880Thr |
| ENST00000619499.4:c.5635G>A | ENSP00000482132.1:p.Ala1879Thr |
| ENST00000703783.1:n.2422G>A | |
| ENST00000703785.1:n.2341G>A | |
| XM_017009228.2:c.5485G>A | XP_016864717.1:p.Ala1829Thr |