Linked Data
gnomAD v4:
15-58749936-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.58749936T>G , CM000677.2:g.58749936T>G | GRCh38 |
| NC_000015.9:g.59042135T>G , CM000677.1:g.59042135T>G | GRCh37 |
| NC_000015.8:g.56829427T>G | NCBI36 |
| NG_033876.1:g.5043A>C | |
| NG_033876.2:g.4772A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260408.7:c.-402A>C | ENSP00000260408.3:n.-402A>C | |
| NM_001110.3:c.-402A>C | NP_001101.1:n.-402A>C | |
| NM_001320570.1:c.-402A>C | NP_001307499.1:n.-402A>C |