Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.68829634G>A , CM000685.2:g.68829634G>A | GRCh38 |
| NC_000023.10:g.68049477G>A , CM000685.1:g.68049477G>A | GRCh37 |
| NC_000023.9:g.67966202G>A | NCBI36 |
| NG_008887.1:g.5638G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000204961.5:c.-143G>A MANE Select | ENSP00000204961.4:n.-143G>A | |
| ENST00000204961.4:c.-143G>A | ENSP00000204961.4:n.-143G>A | |
| NM_004429.4:c.-143G>A | NP_004420.1:n.-143G>A | |
| NM_004429.5:c.-143G>A MANE Select | NP_004420.1:n.-143G>A |