Linked Data
dbSNP Id:
rs558953986
gnomAD v3:
6-28161817-C-T
gnomAD v4:
6-28161817-C-T
MyVariant Identifiers:
chr6:g.28129595C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.28161817C>T , CM000668.2:g.28161817C>T | GRCh38 |
| NC_000006.11:g.28129595C>T , CM000668.1:g.28129595C>T | GRCh37 |
| NC_000006.10:g.28237574C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000562227.2:n.49C>T | ||
| ENST00000440790.6:n.37C>T | ||
| ENST00000570126.1:n.26C>T | ||
| NR_103448.1:n.57C>T |