Linked Data
gnomAD v4:
14-74493599-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.74493599G>T , CM000676.2:g.74493599G>T | GRCh38 |
| NC_000014.8:g.74960302G>T , CM000676.1:g.74960302G>T | GRCh37 |
| NC_000014.7:g.74030055G>T | NCBI36 |
| NG_007117.1:g.4783C>A | |
| NG_033074.1:g.4880G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000555592.1:c.-93C>A | ENSP00000450887.1:n.-93C>A | |
| ENST00000556009.5:c.147+432C>A |