Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.118111528T>A , CM000670.2:g.118111528T>A | GRCh38 |
| NC_000008.10:g.119123767T>A , CM000670.1:g.119123767T>A | GRCh37 |
| NC_000008.9:g.119192948T>A | NCBI36 |
| NG_007455.2:g.5292A>T , LRG_493:g.5292A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378204.7:c.-482A>T MANE Select | ENSP00000367446.3:n.-482A>T | |
| ENST00000378204.6:c.-482A>T | ENSP00000367446.2:n.-482A>T | |
| NM_000127.2:c.-482A>T , LRG_493t1:c.-482A>T | NP_000118.2:n.-482A>T | |
| NM_000127.3:c.-482A>T MANE Select | NP_000118.2:n.-482A>T |