Linked Data
MyVariant Identifiers:
chr6:g.31431785G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31464008G>T , CM000668.2:g.31464008G>T | GRCh38 |
| NC_000006.11:g.31431785G>T , CM000668.1:g.31431785G>T | GRCh37 |
| NC_000006.10:g.31539764G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_040662.1:n.738G>T |