Linked Data
dbSNP Id:
rs1704493388
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.87123990C>T , CM000665.2:g.87123990C>T | GRCh38 |
| NC_000003.11:g.87173140C>T , CM000665.1:g.87173140C>T | GRCh37 |
| NC_000003.10:g.87255830C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_104153.1:n.329-30348C>T |