Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128305921C>A , CM000667.2:g.128305921C>A | GRCh38 |
| NC_000005.9:g.127641613C>A , CM000667.1:g.127641613C>A | GRCh37 |
| NC_000005.8:g.127669512C>A | NCBI36 |
| NG_008750.1:g.237123G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703783.1:n.2234G>T | ||
| ENST00000703785.1:n.2153G>T | ||
| ENST00000262464.9:c.5450G>T MANE Select | ENSP00000262464.4:p.Gly1817Val | |
| ENST00000262464.8:c.5450G>T | ENSP00000262464.4:p.Gly1817Val | |
| ENST00000508053.5:c.5450G>T | ENSP00000424571.1:p.Gly1817Val | |
| ENST00000619499.4:c.5447G>T | ENSP00000482132.1:p.Gly1816Val | |
| NM_001999.3:c.5450G>T | NP_001990.2:p.Gly1817Val | |
| XM_017009228.2:c.5297G>T | XP_016864717.1:p.Gly1766Val | |
| NM_001999.4:c.5450G>T MANE Select | NP_001990.2:p.Gly1817Val |