Linked Data
dbSNP Id:
rs6825911
gnomAD v2:
4-111381638-C-T
gnomAD v3:
4-110460482-C-T
gnomAD v4:
4-110460482-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.110460482C>T , CM000666.2:g.110460482C>T | GRCh38 |
| NC_000004.11:g.111381638C>T , CM000666.1:g.111381638C>T | GRCh37 |
| NC_000004.10:g.111601087C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000510961.1:n.73-28059C>T |