Linked Data
dbSNP Id:
rs1269353092
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31969777G>A , CM000668.2:g.31969777G>A | GRCh38 |
| NC_000006.11:g.31937554G>A , CM000668.1:g.31937554G>A | GRCh37 |
| NC_000006.10:g.32045533G>A | NCBI36 |
| NG_032652.1:g.15974G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461073.6:c.*2851G>A | ENSP00000419905.1:n.*2851G>A | |
| ENST00000697831.1:c.*62G>A | ENSP00000513453.1:n.*62G>A | |
| ENST00000697835.1:c.*3321G>A | ENSP00000513455.1:n.*3321G>A | |
| ENST00000697838.1:c.*62G>A | ENSP00000513457.1:n.*62G>A | |
| XR_926301.3:n.3819G>A |