Linked Data
MyVariant Identifiers:
chr6:g.31362535T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31394758T>A , CM000668.2:g.31394758T>A | GRCh38 |
| NC_000006.11:g.31362535T>A , CM000668.1:g.31362535T>A | GRCh37 |
| NC_000006.10:g.31470514T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_241998.3:n.887A>T | ||
| NR_148222.1:n.877A>T | ||
| NR_148223.1:n.910A>T |