Linked Data
dbSNP Id:
rs1368190446
gnomAD v3:
2-233250122-T-A
gnomAD v4:
2-233250122-T-A
MyVariant Identifiers:
chr2:g.233250122T>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.233250122T>A , CM000664.2:g.233250122T>A | GRCh38 |
| NC_000002.11:g.234158768T>A , CM000664.1:g.234158768T>A | GRCh37 |
| NC_000002.10:g.233823507T>A | NCBI36 |
| NG_023038.1:g.3552T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000431917.5:c.-137-5980T>A | ENSP00000397512.1:n.-137-5980T>A |