Linked Data
dbSNP Id:
rs2227721
gnomAD v3:
17-28370430-C-T
gnomAD v4:
17-28370430-C-T
MyVariant Identifiers:
chr17:g.28370430C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.28370430C>T , CM000679.2:g.28370430C>T | GRCh38 |
| NC_000017.10:g.26697451C>T , CM000679.1:g.26697451C>T | GRCh37 |
| NC_000017.9:g.23721578C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000226218.8:c.-227G>A (VTN) | ENSP00000226218.4:n.-227G>A | |
| ENST00000379061.8:n.170+5265C>T (SARM1) | ||
| ENST00000542029.1:c.-67-160G>A (VTN) | ENSP00000440439.1:n.-67-160G>A |