Linked Data
dbSNP Id:
rs2113762733
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31359208T>C , CM000668.2:g.31359208T>C | GRCh38 |
| NC_000006.11:g.31326985T>C , CM000668.1:g.31326985T>C | GRCh37 |
| NC_000006.10:g.31434964T>C | NCBI36 |
| NG_023187.1:g.3005A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474381.2:n.1271-1527A>G | ||
| ENST00000481849.6:n.1271-1527A>G | ||
| ENST00000497377.6:n.1271-1527A>G | ||
| ENST00000696559.1:c.-203-1527A>G | ENSP00000512717.1:n.-203-1527A>G | |
| ENST00000696560.1:c.-203-1527A>G | ENSP00000512718.1:n.-203-1527A>G | |
| ENST00000696561.1:c.-203-1527A>G | ENSP00000512719.1:n.-203-1527A>G | |
| ENST00000696562.1:c.-135-1915A>G | ENSP00000512720.1:n.-135-1915A>G |