Linked Data
dbSNP Id:
rs965682514
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.16993019T>G , CM000670.2:g.16993019T>G | GRCh38 |
| NC_000008.10:g.16850528T>G , CM000670.1:g.16850528T>G | GRCh37 |
| NC_000008.9:g.16894899T>G | NCBI36 |
| NG_015978.1:g.14147A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000180166.6:c.*53A>C MANE Select | ENSP00000180166.5:n.*53A>C | |
| ENST00000180166.5:c.*53A>C | ENSP00000180166.5:n.*53A>C | |
| ENST00000519941.1:c.393A>C | ||
| NM_019851.2:c.*53A>C | NP_062825.1:n.*53A>C | |
| NM_019851.3:c.*53A>C MANE Select | NP_062825.1:n.*53A>C |