Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23118608G>T , CM000676.2:g.23118608G>T | GRCh38 |
| NC_000014.8:g.23587817G>T , CM000676.1:g.23587817G>T | GRCh37 |
| NC_000014.7:g.22657657G>T | NCBI36 |
| NG_009617.1:g.5658C>A , LRG_45:g.5658C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696121.1:n.453C>A | ||
| ENST00000696122.1:n.230C>A | ||
| ENST00000206513.6:c.484C>A MANE Select | ENSP00000206513.5:p.Pro162Thr | |
| ENST00000206513.5:c.484C>A | ENSP00000206513.5:p.Pro162Thr | |
| NM_001805.3:c.484C>A | NP_001796.2:p.Pro162Thr | |
| XM_011536359.1:c.439C>A | XP_011534661.1:p.Pro147Thr | |
| NM_001805.4:c.484C>A MANE Select | NP_001796.2:p.Pro162Thr |