Linked Data
dbSNP Id:
rs957977077
gnomAD v3:
20-1996047-G-A
gnomAD v4:
20-1996047-G-A
MyVariant Identifiers:
chr20:g.1996047G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.1996047G>A , CM000682.2:g.1996047G>A | GRCh38 |
| NC_000020.10:g.1976693G>A , CM000682.1:g.1976693G>A | GRCh37 |
| NC_000020.9:g.1924693G>A | NCBI36 |
| NG_028027.1:g.3199C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_244229.1:n.1217-10885G>A | ||
| NR_134520.1:n.1253-10885G>A |