Linked Data
ClinVar Variation Id:
1414158
ClinVar RCV Id:
RCV001930381
dbSNP Id:
rs201700546
ExAC:
6:7574919 C / G
gnomAD v3:
6-7574686-C-G
gnomAD v4:
6-7574686-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.7574686C>G , CM000668.2:g.7574686C>G | GRCh38 |
| NC_000006.11:g.7574919C>G , CM000668.1:g.7574919C>G | GRCh37 |
| NC_000006.10:g.7519918C>G | NCBI36 |
| NG_008803.1:g.38050C>G , LRG_423:g.38050C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710359.1:c.2327C>G | ENSP00000518230.1:p.Ala776Gly | |
| ENST00000684395.1:n.968C>G | ||
| ENST00000379802.8:c.2327C>G MANE Select | ENSP00000369129.3:p.Ala776Gly | |
| ENST00000379802.7:c.2327C>G | ENSP00000369129.3:p.Ala776Gly | |
| ENST00000418664.2:c.2327C>G | ENSP00000396591.2:p.Ala776Gly | |
| NM_001008844.1:c.2327C>G | NP_001008844.1:p.Ala776Gly | |
| NM_004415.2:c.2327C>G , LRG_423t1:c.2327C>G | NP_004406.2:p.Ala776Gly | |
| XM_011514323.1:c.2327C>G | XP_011512625.1:p.Ala776Gly | |
| NM_001008844.2:c.2327C>G | NP_001008844.1:p.Ala776Gly | |
| NM_001319034.1:c.2327C>G | NP_001305963.1:p.Ala776Gly | |
| NM_004415.3:c.2327C>G | NP_004406.2:p.Ala776Gly | |
| NM_004415.4:c.2327C>G MANE Select | NP_004406.2:p.Ala776Gly | |
| NM_001008844.3:c.2327C>G | NP_001008844.1:p.Ala776Gly | |
| NM_001319034.2:c.2327C>G | NP_001305963.1:p.Ala776Gly |