Linked Data
MyVariant Identifiers:
chr6:g.31362416C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31394639C>T , CM000668.2:g.31394639C>T | GRCh38 |
| NC_000006.11:g.31362416C>T , CM000668.1:g.31362416C>T | GRCh37 |
| NC_000006.10:g.31470395C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_241998.3:n.1006G>A | ||
| NR_148222.1:n.996G>A | ||
| NR_148223.1:n.1029G>A |