Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.69353381T>C , CM000674.2:g.69353381T>C | GRCh38 |
| NC_000012.11:g.69747161T>C , CM000674.1:g.69747161T>C | GRCh37 |
| NC_000012.10:g.68033428T>C | NCBI36 |
| NG_008195.1:g.10028T>C , LRG_768:g.10028T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261267.7:c.*162T>C MANE Select | ENSP00000261267.2:n.*162T>C | |
| ENST00000261267.6:c.*162T>C | ENSP00000261267.2:n.*162T>C | |
| ENST00000549690.1:c.*116T>C | ENSP00000449898.1:n.*116T>C | |
| NM_000239.2:c.*162T>C , LRG_768t1:c.*162T>C | NP_000230.1:n.*162T>C | |
| NM_000239.3:c.*162T>C MANE Select | NP_000230.1:n.*162T>C |