Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48408663G>A , CM000677.2:g.48408663G>A | GRCh38 |
| NC_000015.9:g.48700860G>A , CM000677.1:g.48700860G>A | GRCh37 |
| NC_000015.8:g.46488152G>A | NCBI36 |
| NG_008805.2:g.242126C>T , LRG_778:g.242126C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682170.1:n.5124C>T | ||
| ENST00000682767.1:n.4240C>T | ||
| ENST00000316623.10:c.*2327C>T MANE Select | ENSP00000325527.5:n.*2327C>T | |
| ENST00000316623.9:c.*2327C>T | ENSP00000325527.5:n.*2327C>T | |
| NM_000138.4:c.*2327C>T , LRG_778t1:c.*2327C>T | NP_000129.3:n.*2327C>T | |
| NM_000138.5:c.*2327C>T MANE Select | NP_000129.3:n.*2327C>T |