Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.28370430C>G , CM000679.2:g.28370430C>G | GRCh38 |
| NC_000017.10:g.26697451C>G , CM000679.1:g.26697451C>G | GRCh37 |
| NC_000017.9:g.23721578C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000226218.8:c.-227G>C (VTN) | ENSP00000226218.4:n.-227G>C | |
| ENST00000379061.8:n.170+5265C>G (SARM1) | ||
| ENST00000542029.1:c.-67-160G>C (VTN) | ENSP00000440439.1:n.-67-160G>C |