Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.129813823C>A , CM000671.2:g.129813823C>A | GRCh38 |
| NC_000009.11:g.132576102C>A , CM000671.1:g.132576102C>A | GRCh37 |
| NC_000009.10:g.131615923C>A | NCBI36 |
| NG_008049.1:g.15340G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000351698.5:c.*149G>T MANE Select | ENSP00000345719.4:n.*149G>T | |
| ENST00000651202.1:c.*416G>T | ENSP00000498222.1:n.*416G>T | |
| ENST00000351698.4:c.*149G>T | ENSP00000345719.4:n.*149G>T | |
| ENST00000474192.1:n.732G>T | ||
| NM_000113.2:c.*149G>T | NP_000104.1:n.*149G>T | |
| XR_929731.3:n.1343G>T | ||
| NM_000113.3:c.*149G>T MANE Select | NP_000104.1:n.*149G>T |