Linked Data
dbSNP Id:
rs1071643
gnomAD v2:
6-31236639-G-C
gnomAD v3:
6-31268862-G-C
gnomAD v4:
6-31268862-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31268862G>C , CM000668.2:g.31268862G>C | GRCh38 |
| NC_000006.11:g.31236639G>C , CM000668.1:g.31236639G>C | GRCh37 |
| NC_000006.10:g.31344618G>C | NCBI36 |
| NG_029422.2:g.8270C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.*307C>G MANE Select | ENSP00000365402.5:n.*307C>G | |
| ENST00000376228.9:c.*307C>G | ENSP00000365402.5:n.*307C>G | |
| ENST00000376237.8:c.*995C>G | ENSP00000365412.4:n.*995C>G | |
| ENST00000383329.7:c.*307C>G | ENSP00000372819.3:n.*307C>G | |
| ENST00000466892.5:n.641C>G | ||
| ENST00000470363.5:n.1166C>G | ||
| ENST00000487245.5:n.1767C>G | ||
| NM_002117.5:c.*307C>G | NP_002108.4:n.*307C>G | |
| NM_002117.6:c.*307C>G MANE Select | NP_002108.4:n.*307C>G |