Linked Data
dbSNP Id:
rs1168452703
gnomAD v3:
2-233250221-C-T
gnomAD v4:
2-233250221-C-T
MyVariant Identifiers:
chr2:g.233250221C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.233250221C>T , CM000664.2:g.233250221C>T | GRCh38 |
| NC_000002.11:g.234158867C>T , CM000664.1:g.234158867C>T | GRCh37 |
| NC_000002.10:g.233823606C>T | NCBI36 |
| NG_023038.1:g.3651C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000431917.5:c.-137-5881C>T | ENSP00000397512.1:n.-137-5881C>T |