Linked Data
dbSNP Id:
rs1858264502
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102798320G>T , CM000673.2:g.102798320G>T | GRCh38 |
| NC_000011.9:g.102669051G>T , CM000673.1:g.102669051G>T | GRCh37 |
| NC_000011.8:g.102174261G>T | NCBI36 |
| NG_011740.1:g.4916C>A | |
| NG_011740.2:g.4916C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371455.7:n.423+198G>T | ||
| ENST00000525739.6:n.682+198G>T | ||
| ENST00000544704.1:n.443+198G>T | ||
| NR_038390.1:n.682+198G>T |