Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218782339C>G , CM000664.2:g.218782339C>G | GRCh38 |
| NC_000002.11:g.219647062C>G , CM000664.1:g.219647062C>G | GRCh37 |
| NC_000002.10:g.219355306C>G | NCBI36 |
| NG_007959.1:g.5591C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258415.9:c.157C>G MANE Select | ENSP00000258415.4:p.Arg53Gly | |
| ENST00000258415.8:c.157C>G | ENSP00000258415.4:p.Arg53Gly | |
| ENST00000445971.1:c.157C>G | ENSP00000404945.1:p.Arg53Gly | |
| ENST00000466602.1:n.166C>G | ||
| ENST00000494263.5:n.591C>G | ||
| NM_000784.3:c.157C>G | NP_000775.1:p.Arg53Gly | |
| XM_017003488.2:c.-73C>G | XP_016858977.1:n.-73C>G | |
| NM_000784.4:c.157C>G MANE Select | NP_000775.1:p.Arg53Gly |