Linked Data
MyVariant Identifiers:
chr10:g.94178903A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.92419146A>T , CM000672.2:g.92419146A>T | GRCh38 |
| NC_000010.10:g.94178903A>T , CM000672.1:g.94178903A>T | GRCh37 |
| NC_000010.9:g.94168883A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000430958.1:n.480A>T | ||
| NR_038243.2:n.486A>T |