Linked Data
dbSNP Id:
rs1588908077
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.44386279T>A , CM000672.2:g.44386279T>A | GRCh38 |
| NC_000010.10:g.44881727T>A , CM000672.1:g.44881727T>A | GRCh37 |
| NC_000010.9:g.44201733T>A | NCBI36 |
| NG_016861.1:g.3819A>T | |
| NG_016861.2:g.3819A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496375.1:n.215A>T |