Linked Data
gnomAD v4:
16-14301442-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.14301442G>T , CM000678.2:g.14301442G>T | GRCh38 |
| NC_000016.9:g.14395299G>T , CM000678.1:g.14395299G>T | GRCh37 |
| NC_000016.8:g.14302800G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_170633.1:n.62G>T |