Linked Data
dbSNP Id:
rs1734716369
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99353041A>G , CM000666.2:g.99353041A>G | GRCh38 |
| NC_000004.11:g.100274198A>G , CM000666.1:g.100274198A>G | GRCh37 |
| NC_000004.10:g.100493221A>G | NCBI36 |
| NG_011718.1:g.4720T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NM_000669.4:c.-366T>C | NP_000660.1:n.-366T>C | |
| NR_133005.1:n.5T>C | ||
| XM_011531589.1:c.-606T>C | XP_011529891.1:n.-606T>C |