Linked Data
dbSNP Id:
rs1718658962
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73404212C>T , CM000666.2:g.73404212C>T | GRCh38 |
| NC_000004.11:g.74269929C>T , CM000666.1:g.74269929C>T | GRCh37 |
| NC_000004.10:g.74488793C>T | NCBI36 |
| NG_009291.1:g.4958C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000441319.5:c.48-157C>T | ENSP00000392541.1:n.48-157C>T |