Linked Data
gnomAD v4:
14-102922638-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.102922638T>C , CM000676.2:g.102922638T>C | GRCh38 |
| NC_000014.8:g.103388975T>C , CM000676.1:g.103388975T>C | GRCh37 |
| NC_000014.7:g.102458728T>C | NCBI36 |
| NG_008276.2:g.4983T>C , LRG_642:g.4983T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011537202.1:c.-232T>C | XP_011535504.1:n.-232T>C | |
| XM_011537202.3:c.-232T>C | XP_011535504.1:n.-232T>C | |
| XM_024449714.1:c.46T>C | XP_024305482.1:p.Trp16Arg |