Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.24956452G>T , CM000670.2:g.24956452G>T | GRCh38 |
| NC_000008.10:g.24813966G>T , CM000670.1:g.24813966G>T | GRCh37 |
| NC_000008.9:g.24869883G>T | NCBI36 |
| NG_008492.1:g.5166C>A , LRG_259:g.5166C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000610854.2:c.64C>A MANE Select | ENSP00000482169.2:p.Pro22Thr | |
| ENST00000610854.1:c.64C>A | ENSP00000482169.1:p.Pro22Thr | |
| ENST00000615973.1:n.270C>A | ||
| ENST00000619417.1:c.64C>A | ENSP00000483690.1:p.Pro22Thr | |
| NM_006158.4:c.64C>A , LRG_259t1:c.64C>A | NP_006149.2:p.Pro22Thr | |
| NM_006158.5:c.64C>A MANE Select | NP_006149.2:p.Pro22Thr |