Linked Data
gnomAD v4:
8-6870582-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.6870582C>T , CM000670.2:g.6870582C>T | GRCh38 |
| NC_000008.10:g.6728104C>T , CM000670.1:g.6728104C>T | GRCh37 |
| NC_000008.9:g.6715514C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000297439.3:c.*99G>A | ENSP00000297439.3:n.*99G>A | |
| NM_005218.3:c.*99G>A | NP_005209.1:n.*99G>A |