Linked Data
gnomAD v4:
14-74493482-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.74493482C>A , CM000676.2:g.74493482C>A | GRCh38 |
| NC_000014.8:g.74960185C>A , CM000676.1:g.74960185C>A | GRCh37 |
| NC_000014.7:g.74029938C>A | NCBI36 |
| NG_007117.1:g.4900G>T | |
| NG_033074.1:g.4763C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000555592.1:c.-64+88G>T | ENSP00000450887.1:n.-64+88G>T | |
| ENST00000555619.5:c.-208G>T | ENSP00000451112.1:n.-208G>T | |
| ENST00000556009.5:c.147+549G>T | ||
| NM_001363688.1:c.-208G>T | NP_001350617.1:n.-208G>T | |
| NM_006432.4:c.-208G>T | NP_006423.1:n.-208G>T |