Linked Data
ClinVar Variation Id:
1942405
ClinVar RCV Id:
RCV002646788
dbSNP Id:
rs753052479
ExAC:
12:49579711 A / C
gnomAD v2:
12-49579711-A-C
gnomAD v4:
12-49185928-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.49185928A>C , CM000674.2:g.49185928A>C | GRCh38 |
| NC_000012.11:g.49579711A>C , CM000674.1:g.49579711A>C | GRCh37 |
| NC_000012.10:g.47865978A>C | NCBI36 |
| NG_008966.1:g.8151T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301071.12:c.438T>G MANE Select | ENSP00000301071.7:p.Gly146= | |
| ENST00000547939.6:c.333T>G | ENSP00000450268.2:p.Gly111= | |
| ENST00000550767.6:c.333T>G | ENSP00000446637.1:p.Gly111= | |
| ENST00000550811.2:n.1471T>G | ||
| ENST00000552924.2:c.333T>G | ENSP00000448725.2:p.Gly111= | |
| ENST00000679733.1:c.461T>G | ENSP00000505459.1:p.Val154Gly | |
| ENST00000295766.9:c.438T>G | ENSP00000439020.2:p.Gly146= | |
| ENST00000301071.11:c.438T>G | ENSP00000301071.7:p.Gly146= | |
| ENST00000546918.1:c.590T>G | ENSP00000446613.1:p.Val197Gly | |
| ENST00000547939.5:c.333T>G | ENSP00000450268.1:p.Gly111= | |
| ENST00000550767.5:c.333T>G | ENSP00000446637.1:p.Gly111= | |
| ENST00000552924.1:c.333T>G | ENSP00000448725.1:p.Gly111= | |
| NM_001270399.1:c.438T>G | NP_001257328.1:p.Gly146= | |
| NM_001270400.1:c.333T>G | NP_001257329.1:p.Gly111= | |
| NM_006009.3:c.438T>G | NP_006000.2:p.Gly146= | |
| NM_006009.4:c.438T>G MANE Select | NP_006000.2:p.Gly146= | |
| NM_001270399.2:c.438T>G | NP_001257328.1:p.Gly146= | |
| NM_001270400.2:c.333T>G | NP_001257329.1:p.Gly111= |