Linked Data
dbSNP Id:
rs1729840193
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99149665G>T , CM000666.2:g.99149665G>T | GRCh38 |
| NC_000004.11:g.100070822G>T , CM000666.1:g.100070822G>T | GRCh37 |
| NC_000004.10:g.100289845G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504581.1:n.170-6885C>A | ||
| NR_037884.1:n.680-4880G>T |