Linked Data
gnomAD v4:
15-72376039-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.72376039C>A , CM000677.2:g.72376039C>A | GRCh38 |
| NC_000015.9:g.72668380C>A , CM000677.1:g.72668380C>A | GRCh37 |
| NC_000015.8:g.70455434C>A | NCBI36 |
| NG_009017.1:g.5141G>T | |
| NG_009017.2:g.5141G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268097.9:c.-67G>T | ENSP00000268097.5:n.-67G>T | |
| ENST00000569509.5:n.147-208G>T | ||
| NM_000520.4:c.-67G>T | NP_000511.2:n.-67G>T | |
| NM_000520.5:c.-67G>T | NP_000511.2:n.-67G>T | |
| NM_001318825.1:c.-67G>T | NP_001305754.1:n.-67G>T | |
| NR_134869.1:n.435G>T |