Linked Data
dbSNP Id:
rs11648796
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.742190A>T , CM000678.2:g.742190A>T | GRCh38 |
| NC_000016.9:g.792190A>T , CM000678.1:g.792190A>T | GRCh37 |
| NC_000016.8:g.732191A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000620831.4:c.-49-20442A>T | ENSP00000482893.1:n.-49-20442A>T |