Linked Data
MyVariant Identifiers:
chr15:g.45544248A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.45252050A>T , CM000677.2:g.45252050A>T | GRCh38 |
| NC_000015.9:g.45544248A>T , CM000677.1:g.45544248A>T | GRCh37 |
| NC_000015.8:g.43331540A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_120335.1:n.203T>A |