Linked Data
gnomAD v4:
14-102922646-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.102922646G>T , CM000676.2:g.102922646G>T | GRCh38 |
| NC_000014.8:g.103388983G>T , CM000676.1:g.103388983G>T | GRCh37 |
| NC_000014.7:g.102458736G>T | NCBI36 |
| NG_008276.2:g.4991G>T , LRG_642:g.4991G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011537202.1:c.-224G>T | XP_011535504.1:n.-224G>T | |
| XM_011537202.3:c.-224G>T | XP_011535504.1:n.-224G>T | |
| XM_024449714.1:c.54G>T | XP_024305482.1:p.Gln18His |