Linked Data
dbSNP Id:
rs1603640920
gnomAD v4:
10-77781135-C-G
MyVariant Identifiers:
chr10:g.79540893C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.77781135C>G , CM000672.2:g.77781135C>G | GRCh38 |
| NC_000010.10:g.79540893C>G , CM000672.1:g.79540893C>G | GRCh37 |
| NC_000010.9:g.79210899C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000439688.1:n.742G>C |