Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.74493493A>T , CM000676.2:g.74493493A>T | GRCh38 |
| NC_000014.8:g.74960196A>T , CM000676.1:g.74960196A>T | GRCh37 |
| NC_000014.7:g.74029949A>T | NCBI36 |
| NG_007117.1:g.4889T>A | |
| NG_033074.1:g.4774A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000555592.1:c.-64+77T>A | ENSP00000450887.1:n.-64+77T>A | |
| ENST00000555619.5:c.-219T>A | ENSP00000451112.1:n.-219T>A | |
| ENST00000556009.5:c.147+538T>A | ||
| NM_001363688.1:c.-219T>A | NP_001350617.1:n.-219T>A | |
| NM_006432.4:c.-219T>A | NP_006423.1:n.-219T>A |