Linked Data
gnomAD v4:
14-74493529-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.74493529C>G , CM000676.2:g.74493529C>G | GRCh38 |
| NC_000014.8:g.74960232C>G , CM000676.1:g.74960232C>G | GRCh37 |
| NC_000014.7:g.74029985C>G | NCBI36 |
| NG_007117.1:g.4853G>C | |
| NG_033074.1:g.4810C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000555592.1:c.-64+41G>C | ENSP00000450887.1:n.-64+41G>C | |
| ENST00000556009.5:c.147+502G>C |