Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.98541754A>G , CM000671.2:g.98541754A>G | GRCh38 |
| NC_000009.11:g.101304036A>G , CM000671.1:g.101304036A>G | GRCh37 |
| NC_000009.10:g.100343857A>G | NCBI36 |
| NG_016426.1:g.172444T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259455.4:c.630+119T>C MANE Select | ENSP00000259455.2:n.630+119T>C | |
| ENST00000637410.1:n.408+119T>C | ||
| ENST00000259455.3:c.630+119T>C | ENSP00000259455.2:n.630+119T>C | |
| ENST00000477471.1:n.417+119T>C | ||
| ENST00000634227.1:n.404+119T>C | ||
| NM_005458.7:c.630+119T>C | NP_005449.5:n.630+119T>C | |
| XM_017015331.2:c.336+119T>C | XP_016870820.1:n.336+119T>C | |
| NM_005458.8:c.630+119T>C MANE Select | NP_005449.5:n.630+119T>C |