Linked Data
dbSNP Id:
rs1489083163
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.74493567C>G , CM000676.2:g.74493567C>G | GRCh38 |
| NC_000014.8:g.74960270C>G , CM000676.1:g.74960270C>G | GRCh37 |
| NC_000014.7:g.74030023C>G | NCBI36 |
| NG_007117.1:g.4815G>C | |
| NG_033074.1:g.4848C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000555592.1:c.-64+3G>C | ENSP00000450887.1:n.-64+3G>C | |
| ENST00000556009.5:c.147+464G>C |