Canonical Allele Identifier:
CA880474198
Gene:
Linked Data
dbSNP Id:
rs1288540397
gnomAD v3:
19-20217925-T-G
gnomAD v4:
19-20217925-T-G
MyVariant Identifiers:
chr19:g.20217925T>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.20217925T>G , CM000681.2:g.20217925T>G | GRCh38 |
| NC_000019.9:g.20328734T>G , CM000681.1:g.20328734T>G | GRCh37 |
| NC_000019.8:g.20189734T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_936388.1:n.619-609A>C | ||
| XR_936389.1:n.502-609A>C | ||
| XR_936390.1:n.511-609A>C | ||
| XR_936391.1:n.514-609A>C | ||
| XR_936392.1:n.514-609A>C | ||
| XR_936394.1:n.41-809T>G | ||
| XR_001754063.2:n.1506-609A>C | ||
| XR_001754064.2:n.138-609A>C | ||
| XR_001754066.1:n.3912-609A>C | ||
| XR_001754067.1:n.3912-609A>C | ||
| XR_001754068.1:n.3912-609A>C | ||
| XR_936394.2:n.41-809T>G | ||
| XR_936406.2:n.1411-609A>C |