Linked Data
dbSNP Id:
rs1827686608
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.115381571G>A , CM000671.2:g.115381571G>A | GRCh38 |
| NC_000009.11:g.118143850G>A , CM000671.1:g.118143850G>A | GRCh37 |
| NC_000009.10:g.117183671G>A | NCBI36 |
| NG_027530.1:g.244754G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000374016.5:c.13+4856G>A | ENSP00000363128.1:n.13+4856G>A | |
| NM_017418.2:c.13+4856G>A | NP_059114.1:n.13+4856G>A | |
| XM_011518753.1:c.13+4856G>A | XP_011517055.1:n.13+4856G>A | |
| NR_163556.1:n.535+4856G>A |