Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107696043A>G , CM000669.2:g.107696043A>G | GRCh38 |
| NC_000007.13:g.107336488A>G , CM000669.1:g.107336488A>G | GRCh37 |
| NC_000007.12:g.107123724A>G | NCBI36 |
| NG_008489.1:g.40409A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644269.2:c.1544+4A>G MANE Select | ENSP00000494017.1:n.1544+4A>G | |
| ENST00000644846.1:c.255+4A>G | ||
| ENST00000265715.7:c.1544+4A>G | ENSP00000265715.3:n.1544+4A>G | |
| ENST00000477350.5:n.391+4A>G | ||
| ENST00000480841.5:n.393+4A>G | ||
| NM_000441.1:c.1544+4A>G | NP_000432.1:n.1544+4A>G | |
| XM_005250425.1:c.1544+4A>G | XP_005250482.1:n.1544+4A>G | |
| XM_005250425.2:c.1544+4A>G | XP_005250482.1:n.1544+4A>G | |
| XM_017012318.1:c.1466+4A>G | XP_016867807.1:n.1466+4A>G | |
| NM_000441.2:c.1544+4A>G MANE Select | NP_000432.1:n.1544+4A>G |