Linked Data
gnomAD v4:
21-31659658-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.31659658C>T , CM000683.2:g.31659658C>T | GRCh38 |
| NC_000021.8:g.33031971C>T , CM000683.1:g.33031971C>T | GRCh37 |
| NC_000021.7:g.31953842C>T | NCBI36 |
| NG_008689.1:g.5037C>T , LRG_652:g.5037C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270142.10:c.-112C>T | ENSP00000270142.6:n.-112C>T | |
| NM_000454.4:c.-112C>T , LRG_652t1:c.-112C>T | NP_000445.1:n.-112C>T |