Linked Data
gnomAD v4:
6-35797488-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.35797488T>A , CM000668.2:g.35797488T>A | GRCh38 |
| NC_000006.11:g.35765265T>A , CM000668.1:g.35765265T>A | GRCh37 |
| NC_000006.10:g.35873243T>A | NCBI36 |
| NG_012184.3:g.5283T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651132.1:c.-255+29T>A | ENSP00000498322.1:n.-255+29T>A | |
| XM_011514403.1:c.-135+29T>A | XP_011512705.1:n.-135+29T>A |