Linked Data
dbSNP Id:
rs1596911333
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.142391929C>T , CM000667.2:g.142391929C>T | GRCh38 |
| NC_000005.9:g.141771494C>T , CM000667.1:g.141771494C>T | GRCh37 |
| NC_000005.8:g.141751678C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_120664.1:n.506+38346C>T |