Linked Data
dbSNP Id:
rs1051901283
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47403029G>C , CM000664.2:g.47403029G>C | GRCh38 |
| NC_000002.11:g.47630168G>C , CM000664.1:g.47630168G>C | GRCh37 |
| NC_000002.10:g.47483672G>C | NCBI36 |
| NG_007110.2:g.4906G>C , LRG_218:g.4906G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233146.6:c.-163G>C | ENSP00000233146.2:n.-163G>C |