Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186085557G>T , CM000666.2:g.186085557G>T | GRCh38 |
| NC_000004.11:g.187006711G>T , CM000666.1:g.187006711G>T | GRCh37 |
| NC_000004.10:g.187243705G>T | NCBI36 |
| NG_007278.1:g.21403G>T , LRG_117:g.21403G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000698352.1:c.*2951G>T | ENSP00000513675.1:n.*2951G>T | |
| ENST00000698353.1:n.3274G>T | ||
| ENST00000698354.1:c.*684G>T | ENSP00000513676.1:n.*684G>T | |
| ENST00000296795.8:c.*684G>T MANE Select | ENSP00000296795.3:n.*684G>T | |
| ENST00000296795.7:c.*684G>T | ENSP00000296795.2:n.*684G>T | |
| NM_003265.3:c.*684G>T MANE Select | NP_003256.1:n.*684G>T |