Linked Data
dbSNP Id:
rs1946710483
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.47910790C>T , CM000674.2:g.47910790C>T | GRCh38 |
| NC_000012.11:g.48304573C>T , CM000674.1:g.48304573C>T | GRCh37 |
| NC_000012.10:g.46590840C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395324.6:c.-83-28016G>A | ENSP00000378734.2:n.-83-28016G>A |