Linked Data
dbSNP Id:
rs1762840234
gnomAD v3:
6-31463642-C-T
gnomAD v4:
6-31463642-C-T
MyVariant Identifiers:
chr6:g.31431419C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31463642C>T , CM000668.2:g.31463642C>T | GRCh38 |
| NC_000006.11:g.31431419C>T , CM000668.1:g.31431419C>T | GRCh37 |
| NC_000006.10:g.31539398C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_040662.1:n.372C>T |