Linked Data
dbSNP Id:
rs982972026
gnomAD v4:
17-35880698-G-A
MyVariant Identifiers:
chr17:g.35880698G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.35880698G>A , CM000679.2:g.35880698G>A | GRCh38 |
| NC_000017.9:g.31231815G>A | NCBI36 |
| NG_015990.1:g.4676C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000605509.2:c.-18+31C>T | ENSP00000474141.2:n.-18+31C>T | |
| ENST00000605140.5:c.-18+31C>T | ENSP00000475057.1:n.-18+31C>T | |
| XR_934696.1:n.197-3684G>A | ||
| XR_934697.1:n.200-3684G>A | ||
| XR_001752852.1:n.426+624G>A | ||
| XR_934696.2:n.91-3684G>A | ||
| XR_934697.2:n.91-3684G>A |