Linked Data
gnomAD v4:
14-60649527-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.60649527C>A , CM000676.2:g.60649527C>A | GRCh38 |
| NC_000014.8:g.61116245C>A , CM000676.1:g.61116245C>A | GRCh37 |
| NC_000014.7:g.60185998C>A | NCBI36 |
| NG_008231.1:g.4911G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553535.2:n.248+2408G>T | ||
| ENST00000554986.2:c.42-2950G>T | ENSP00000452700.2:n.42-2950G>T | |
| ENST00000555955.3:n.1197+2408G>T |