Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.64833125C>G , CM000663.2:g.64833125C>G | GRCh38 |
| NC_000001.10:g.65298808C>G , CM000663.1:g.65298808C>G | GRCh37 |
| NC_000001.9:g.65071396C>G | NCBI36 |
| NG_023402.1:g.138380G>C | |
| NG_023402.2:g.239622G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000294428.8:c.*2140C>G MANE Select | ENSP00000294428.3:n.*2140C>G | |
| ENST00000294428.7:c.*2140C>G | ENSP00000294428.3:n.*2140C>G | |
| ENST00000371072.8:c.*2140C>G | ENSP00000360112.4:n.*2140C>G | |
| NM_018211.3:c.*2140C>G | NP_060681.2:n.*2140C>G | |
| XM_006710738.2:c.*2140C>G | XP_006710801.2:n.*2140C>G | |
| NM_001366165.1:c.*2140C>G | NP_001353094.1:n.*2140C>G | |
| XR_946693.3:n.4559C>G | ||
| NM_018211.4:c.*2140C>G | NP_060681.2:n.*2140C>G | |
| NM_001366165.2:c.*2140C>G MANE Select | NP_001353094.1:n.*2140C>G |