Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.72243608A>T , CM000673.2:g.72243608A>T | GRCh38 |
| NC_000011.9:g.71954652A>T , CM000673.1:g.71954652A>T | GRCh37 |
| NC_000011.8:g.71632300A>T | NCBI36 |
| NG_008169.1:g.5569T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000298231.5:c.217+180T>A MANE Select | ENSP00000298231.5:n.217+180T>A | |
| ENST00000544057.1:n.85+1972T>A | ||
| NM_005169.3:c.217+180T>A | NP_005160.2:n.217+180T>A | |
| NM_005169.4:c.217+180T>A MANE Select | NP_005160.2:n.217+180T>A |