Linked Data
gnomAD v4:
19-39247569-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.39247569C>A , CM000681.2:g.39247569C>A | GRCh38 |
| NC_000019.9:g.39738209C>A , CM000681.1:g.39738209C>A | GRCh37 |
| NC_000019.8:g.44430049C>A | NCBI36 |
| NG_042193.1:g.2403G>T | |
| NG_055295.1:g.6288G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000606380.2:c.368-106G>T | ENSP00000476098.1:n.368-106G>T | |
| ENST00000610963.1:c.367-106G>T | ENSP00000481371.1:n.367-106G>T | |
| ENST00000616270.4:c.321G>T | ENSP00000480679.1:p.Gly107= | |
| ENST00000634680.1:c.152-106G>T | ENSP00000489240.1:n.152-106G>T | |
| ENST00000634967.1:c.224-106G>T | ENSP00000489559.1:n.224-106G>T | |
| NR_074079.1:n.645-106G>T |