Linked Data
dbSNP Id:
rs1217252007
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.150155870T>C , CM000667.2:g.150155870T>C | GRCh38 |
| NC_000005.9:g.149535433T>C , CM000667.1:g.149535433T>C | GRCh37 |
| NC_000005.8:g.149515626T>C | NCBI36 |
| NG_023367.1:g.4990A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000523456.1:n.3A>G | ||
| XM_005268464.2:c.-626A>G | XP_005268521.1:n.-626A>G | |
| XM_011537659.1:c.-947A>G | XP_011535961.1:n.-947A>G |