Linked Data
dbSNP Id:
rs1420416168
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.157110522T>C , CM000667.2:g.157110522T>C | GRCh38 |
| NC_000005.9:g.156537533T>C , CM000667.1:g.156537533T>C | GRCh37 |
| NC_000005.8:g.156470111T>C | NCBI36 |
| NG_030444.1:g.3716A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000524219.2:c.-293-3560A>G | ENSP00000430328.2:n.-293-3560A>G | |
| ENST00000696899.1:c.-264-1275A>G | ENSP00000512960.1:n.-264-1275A>G | |
| ENST00000524219.1:c.-293-3560A>G | ENSP00000430328.1:n.-293-3560A>G |