Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.10752774A>T , CM000673.2:g.10752774A>T | GRCh38 |
| NC_000011.9:g.10774321A>T , CM000673.1:g.10774321A>T | GRCh37 |
| NC_000011.8:g.10730897A>T | NCBI36 |
| NG_051671.1:g.6788A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_014633.5:c.144+4A>T MANE Select | NP_055448.1:n.144+4A>T |
| ENST00000361367.7:c.144+4A>T MANE Select | ENSP00000355013.2:n.144+4A>T |
| NM_001346279.1:c.144+4A>T | NP_001333208.1:n.144+4A>T |
| NM_001346279.2:c.144+4A>T | NP_001333208.1:n.144+4A>T |
| NM_014633.4:c.144+4A>T | NP_055448.1:n.144+4A>T |
| ENST00000361367.6:c.144+4A>T | ENSP00000355013.2:n.144+4A>T |
| ENST00000524523.1:c.105+4A>T | ENSP00000431458.1:n.105+4A>T |