Linked Data
dbSNP Id:
rs1379670479
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.13316188C>T , CM000682.2:g.13316188C>T | GRCh38 |
| NC_000020.10:g.13296835C>T , CM000682.1:g.13296835C>T | GRCh37 |
| NC_000020.9:g.13244835C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_937280.1:n.601-133G>A | ||
| XM_017027680.1:c.878-8878C>T (ISM1) | XP_016883169.1:n.878-8878C>T | |
| XR_001754319.2:n.1282-133G>A (TASP1) |