Linked Data
dbSNP Id:
rs2152113783
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68737254T>C , CM000678.2:g.68737254T>C | GRCh38 |
| NC_000016.9:g.68771157T>C , CM000678.1:g.68771157T>C | GRCh37 |
| NC_000016.8:g.67328658T>C | NCBI36 |
| NG_008021.1:g.4963T>C , LRG_301:g.4963T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261769.9:c.-162T>C | ENSP00000261769.4:n.-162T>C |