Linked Data
dbSNP Id:
rs1765947315
gnomAD v3:
6-28161821-G-T
gnomAD v4:
6-28161821-G-T
MyVariant Identifiers:
chr6:g.28129599G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.28161821G>T , CM000668.2:g.28161821G>T | GRCh38 |
| NC_000006.11:g.28129599G>T , CM000668.1:g.28129599G>T | GRCh37 |
| NC_000006.10:g.28237578G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000562227.2:n.53G>T | ||
| ENST00000440790.6:n.41G>T | ||
| ENST00000570126.1:n.30G>T | ||
| NR_103448.1:n.61G>T |