Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.44114490G>T , CM000669.2:g.44114490G>T | GRCh38 |
| NC_000007.13:g.44154089G>T , CM000669.1:g.44154089G>T | GRCh37 |
| NC_000007.12:g.44120614G>T | NCBI36 |
| NG_056775.1:g.15171G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001129.5:c.*229G>T MANE Select | NP_001120.3:n.*229G>T |
| ENST00000223357.8:c.*229G>T MANE Select | ENSP00000223357.3:n.*229G>T |
| NM_001129.4:c.*229G>T | NP_001120.3:n.*229G>T |
| ENST00000223357.7:c.*229G>T | ENSP00000223357.3:n.*229G>T |
| ENST00000413907.1:c.2103G>T | |
| ENST00000450684.2:c.*229G>T | ENSP00000398878.2:n.*229G>T |
| XM_011515162.1:c.*229G>T | XP_011513464.1:n.*229G>T |