Linked Data
dbSNP Id:
rs773503730
gnomAD v3:
17-35880786-C-T
gnomAD v4:
17-35880786-C-T
MyVariant Identifiers:
chr17:g.35880786C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.35880786C>T , CM000679.2:g.35880786C>T | GRCh38 |
| NC_000017.9:g.31231903C>T | NCBI36 |
| NG_015990.1:g.4588G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000605509.2:c.-75G>A | ENSP00000474141.2:n.-75G>A | |
| ENST00000605140.5:c.-75G>A | ENSP00000475057.1:n.-75G>A | |
| XR_934696.1:n.197-3596C>T | ||
| XR_934697.1:n.200-3596C>T | ||
| XR_001752852.1:n.426+712C>T | ||
| XR_934696.2:n.91-3596C>T | ||
| XR_934697.2:n.91-3596C>T |