Linked Data
gnomAD v4:
4-99144315-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99144315C>T , CM000666.2:g.99144315C>T | GRCh38 |
| NC_000004.11:g.100065466C>T , CM000666.1:g.100065466C>T | GRCh37 |
| NC_000004.10:g.100284489C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504581.1:n.170-1535G>A | ||
| NR_037884.1:n.680-10230C>T |