Linked Data
ClinVar Variation Id:
182563
dbSNP Id:
rs587782355
ExAC:
2:47693816 G / C
gnomAD v2:
2-47693816-G-C
gnomAD v3:
2-47466677-G-C
gnomAD v4:
2-47466677-G-C
COSMIC:
COSM1483118
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47466677G>C , CM000664.2:g.47466677G>C | GRCh38 |
| NC_000002.11:g.47693816G>C , CM000664.1:g.47693816G>C | GRCh37 |
| NC_000002.10:g.47547320G>C | NCBI36 |
| NG_007110.2:g.68554G>C , LRG_218:g.68554G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000644900.2:c.1530G>C | ENSP00000495641.2:p.Gln510His | |
| ENST00000233146.7:c.1530G>C MANE Select | ENSP00000233146.2:p.Gln510His | |
| ENST00000543555.6:c.1332G>C | ENSP00000442697.1:p.Gln444His | |
| ENST00000644092.1:c.1530G>C | ENSP00000496351.1:p.Gln510His | |
| ENST00000645339.1:c.1530G>C | ENSP00000496441.1:p.Gln510His | |
| ENST00000645506.1:c.1530G>C | ENSP00000495455.1:p.Gln510His | |
| ENST00000646415.1:c.1530G>C | ENSP00000495543.1:p.Gln510His | |
| ENST00000233146.6:c.1530G>C | ENSP00000233146.2:p.Gln510His | |
| ENST00000406134.5:c.1530G>C | ENSP00000384199.1:p.Gln510His | |
| ENST00000543555.5:c.1332G>C | ENSP00000442697.1:p.Gln444His | |
| ENST00000610696.4:c.1530G>C | ENSP00000483159.1:p.Gln510His | |
| ENST00000613514.4:c.*70G>C | ENSP00000484137.1:n.*70G>C | |
| ENST00000617333.3:c.*296G>C | ENSP00000482468.1:n.*296G>C | |
| ENST00000617938.4:c.*502G>C | ENSP00000481158.1:n.*502G>C | |
| ENST00000621359.2:c.1530G>C | ENSP00000481416.1:p.Gln510His | |
| NM_000251.2:c.1530G>C , LRG_218t1:c.1530G>C | NP_000242.1:p.Gln510His | |
| NM_001258281.1:c.1332G>C | NP_001245210.1:p.Gln444His | |
| XM_005264332.2:c.1530G>C | XP_005264389.2:p.Gln510His | |
| XM_011532867.1:c.1530G>C | XP_011531169.1:p.Gln510His | |
| XR_939685.1:n.1602G>C | ||
| XM_005264332.4:c.1530G>C | XP_005264389.2:p.Gln510His | |
| XM_011532867.2:c.1530G>C | XP_011531169.1:p.Gln510His | |
| XR_001738747.2:n.1592G>C | ||
| XR_939685.2:n.1592G>C | ||
| NM_000251.3:c.1530G>C MANE Select | NP_000242.1:p.Gln510His |