Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24347892A>T , CM000668.2:g.24347892A>T | GRCh38 |
| NC_000006.11:g.24348120A>T , CM000668.1:g.24348120A>T | GRCh37 |
| NC_000006.10:g.24456099A>T | NCBI36 |
| NG_012829.1:g.15161T>A | |
| NG_012829.2:g.40401T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000378454.8:c.348+5677T>A MANE Select | ENSP00000367715.3:n.348+5677T>A | |
| ENST00000378454.7:c.348+5677T>A | ENSP00000367715.3:n.348+5677T>A | |
| NM_001195610.1:c.348+5677T>A | NP_001182539.1:n.348+5677T>A | |
| NM_016356.4:c.348+5677T>A | NP_057440.2:n.348+5677T>A | |
| NM_016356.5:c.348+5677T>A MANE Select | NP_057440.2:n.348+5677T>A | |
| NM_001195610.2:c.348+5677T>A | NP_001182539.1:n.348+5677T>A |