Linked Data
dbSNP Id:
rs1776820712
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.112069767A>G , CM000668.2:g.112069767A>G | GRCh38 |
| NC_000006.11:g.112390970A>G , CM000668.1:g.112390970A>G | GRCh37 |
| NC_000006.10:g.112497663A>G | NCBI36 |
| NG_011748.1:g.20693A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361714.5:c.*147A>G | ENSP00000354734.2:n.*147A>G | |
| ENST00000368666.6:c.*147A>G | ENSP00000357655.3:n.*147A>G |