Linked Data
MyVariant Identifiers:
chr16:g.52586248A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.52552336A>C , CM000678.2:g.52552336A>C | GRCh38 |
| NC_000016.9:g.52586248A>C , CM000678.1:g.52586248A>C | GRCh37 |
| NC_000016.8:g.51143749A>C | NCBI36 |
| NG_012623.1:g.467T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_033920.1:n.752T>G |