Canonical Allele Identifier:
CA880474197
Gene:
Linked Data
dbSNP Id:
rs1488852291
gnomAD v3:
19-20217914-G-T
gnomAD v4:
19-20217914-G-T
MyVariant Identifiers:
chr19:g.20217914G>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.20217914G>T , CM000681.2:g.20217914G>T | GRCh38 |
| NC_000019.9:g.20328723G>T , CM000681.1:g.20328723G>T | GRCh37 |
| NC_000019.8:g.20189723G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_936388.1:n.619-598C>A | ||
| XR_936389.1:n.502-598C>A | ||
| XR_936390.1:n.511-598C>A | ||
| XR_936391.1:n.514-598C>A | ||
| XR_936392.1:n.514-598C>A | ||
| XR_936394.1:n.41-820G>T | ||
| XR_001754063.2:n.1506-598C>A | ||
| XR_001754064.2:n.138-598C>A | ||
| XR_001754066.1:n.3912-598C>A | ||
| XR_001754067.1:n.3912-598C>A | ||
| XR_001754068.1:n.3912-598C>A | ||
| XR_936394.2:n.41-820G>T | ||
| XR_936406.2:n.1411-598C>A |