Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.24952658C>A , CM000670.2:g.24952658C>A | GRCh38 |
| NC_000008.10:g.24810171C>A , CM000670.1:g.24810171C>A | GRCh37 |
| NC_000008.9:g.24866088C>A | NCBI36 |
| NG_008492.1:g.8960G>T , LRG_259:g.8960G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000610854.2:c.*152G>T MANE Select | ENSP00000482169.2:n.*152G>T | |
| ENST00000610854.1:c.*152G>T | ENSP00000482169.1:n.*152G>T | |
| ENST00000619417.1:c.*649G>T | ENSP00000483690.1:n.*649G>T | |
| NM_006158.4:c.*152G>T , LRG_259t1:c.*152G>T | NP_006149.2:n.*152G>T | |
| NM_006158.5:c.*152G>T MANE Select | NP_006149.2:n.*152G>T |