Linked Data
ClinVar Variation Id:
2767192
ClinVar RCV Id:
RCV003573780
dbSNP Id:
rs777005322
gnomAD v4:
6-42960968-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.42960968C>G , CM000668.2:g.42960968C>G | GRCh38 |
| NC_000006.11:g.42928706C>G , CM000668.1:g.42928706C>G | GRCh37 |
| NC_000006.10:g.43036684C>G | NCBI36 |
| NG_008396.1:g.5207C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372808.4:c.201C>G MANE Select | ENSP00000361894.3:p.Gly67= | |
| ENST00000372808.3:c.201C>G | ENSP00000361894.3:p.Gly67= | |
| NM_018960.4:c.201C>G | NP_061833.1:p.Gly67= | |
| XM_011514493.1:c.-13-1244C>G | XP_011512795.1:n.-13-1244C>G | |
| XM_011514494.1:c.-13-1244C>G | XP_011512796.1:n.-13-1244C>G | |
| NM_001318856.1:c.9-1244C>G | NP_001305785.1:n.9-1244C>G | |
| NM_001318857.1:c.152-1794C>G | NP_001305786.1:n.152-1794C>G | |
| NM_001318858.1:c.152-1794C>G | NP_001305787.1:n.152-1794C>G | |
| NM_001318865.1:c.201C>G | NP_001305794.1:p.Gly67= | |
| NM_018960.5:c.201C>G | NP_061833.1:p.Gly67= | |
| NR_134890.1:n.690-1794C>G | ||
| NR_134891.1:n.593-1794C>G | ||
| NR_134892.1:n.593-1244C>G | ||
| NR_134899.1:n.215C>G | ||
| NM_018960.6:c.201C>G MANE Select | NP_061833.1:p.Gly67= | |
| NM_001318856.2:c.9-1244C>G | NP_001305785.1:n.9-1244C>G | |
| NM_001318857.2:c.152-1794C>G | NP_001305786.1:n.152-1794C>G | |
| NM_001318858.2:c.152-1794C>G | NP_001305787.1:n.152-1794C>G | |
| NM_001318865.2:c.201C>G | NP_001305794.1:p.Gly67= | |
| NR_134890.2:n.340-1794C>G | ||
| NR_134891.2:n.243-1794C>G | ||
| NR_134892.2:n.243-1244C>G | ||
| NR_134899.2:n.215C>G |