Linked Data
dbSNP Id:
rs4553808
gnomAD v3:
2-203866282-A-T
gnomAD v4:
2-203866282-A-T
MyVariant Identifiers:
chr2:g.203866282A>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.203866282A>T , CM000664.2:g.203866282A>T | GRCh38 |
| NC_000002.11:g.204731005A>T , CM000664.1:g.204731005A>T | GRCh37 |
| NC_000002.10:g.204439250A>T | NCBI36 |
| NG_011502.1:g.3497A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696479.1:c.48-1636A>T | ENSP00000512655.1:n.48-1636A>T |