Linked Data
dbSNP Id:
rs1792683772
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.147795958G>C , CM000668.2:g.147795958G>C | GRCh38 |
| NC_000006.11:g.148117094G>C , CM000668.1:g.148117094G>C | GRCh37 |
| NC_000006.10:g.148158787G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_017010850.1:c.460-151514G>C | XP_016866339.1:n.460-151514G>C |