Linked Data
dbSNP Id:
rs1880208624
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.91111705C>T , CM000674.2:g.91111705C>T | GRCh38 |
| NC_000012.11:g.91505482C>T , CM000674.1:g.91505482C>T | GRCh37 |
| NC_000012.10:g.90029613C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266718.4:c.-329G>A | ENSP00000266718.4:n.-329G>A | |
| NM_002345.3:c.-329G>A | NP_002336.1:n.-329G>A |