Linked Data
dbSNP Id:
rs1667193478
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31586914A>G , CM000664.2:g.31586914A>G | GRCh38 |
| NC_000002.11:g.31811983A>G , CM000664.1:g.31811983A>G | GRCh37 |
| NC_000002.10:g.31665487A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011533070.1:c.27-53148T>C | XP_011531372.1:n.27-53148T>C | |
| XM_011533071.1:c.27-53148T>C | XP_011531373.1:n.27-53148T>C | |
| XM_011533072.1:c.27-53148T>C | XP_011531374.1:n.27-53148T>C | |
| XM_011533072.2:c.27-53148T>C | XP_011531374.1:n.27-53148T>C |