Linked Data
dbSNP Id:
rs1839816368
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.44386213C>T , CM000672.2:g.44386213C>T | GRCh38 |
| NC_000010.10:g.44881661C>T , CM000672.1:g.44881661C>T | GRCh37 |
| NC_000010.9:g.44201667C>T | NCBI36 |
| NG_016861.1:g.3885G>A | |
| NG_016861.2:g.3885G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496375.1:n.281G>A |