Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.135031330C>G , CM000667.2:g.135031330C>G | GRCh38 |
| NC_000005.9:g.134367020C>G , CM000667.1:g.134367020C>G | GRCh37 |
| NC_000005.8:g.134394919C>G | NCBI36 |
| NG_012114.1:g.7945G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265340.12:c.348G>C MANE Select | ENSP00000265340.6:p.Met116Ile | |
| ENST00000265340.11:c.348G>C | ENSP00000265340.6:p.Met116Ile | |
| ENST00000503586.1:c.470G>C | ||
| ENST00000504936.1:n.681G>C | ||
| ENST00000506438.5:c.348G>C | ENSP00000427542.1:p.Met116Ile | |
| ENST00000507253.5:c.348G>C | ENSP00000422908.1:p.Met116Ile | |
| NM_002653.4:c.348G>C | NP_002644.4:p.Met116Ile | |
| NM_002653.5:c.348G>C MANE Select | NP_002644.4:p.Met116Ile |