Linked Data
dbSNP Id:
rs2103857090
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47403018T>C , CM000664.2:g.47403018T>C | GRCh38 |
| NC_000002.11:g.47630157T>C , CM000664.1:g.47630157T>C | GRCh37 |
| NC_000002.10:g.47483661T>C | NCBI36 |
| NG_007110.2:g.4895T>C , LRG_218:g.4895T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233146.6:c.-174T>C | ENSP00000233146.2:n.-174T>C |