Linked Data
MyVariant Identifiers:
chr10:g.101287672A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.99527915A>C , CM000672.2:g.99527915A>C | GRCh38 |
| NC_000010.10:g.101287672A>C , CM000672.1:g.101287672A>C | GRCh37 |
| NC_000010.9:g.101277662A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_120618.1:n.468T>G |