Linked Data
ClinVar Variation Id:
2798971
ClinVar RCV Id:
RCV003668254
dbSNP Id:
rs1189348356
gnomAD v4:
2-1477454-C-T
MyVariant Identifiers:
chr2:g.1481226C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.1477454C>T , CM000664.2:g.1477454C>T | GRCh38 |
| NC_000002.11:g.1481226C>T , CM000664.1:g.1481226C>T | GRCh37 |
| NC_000002.10:g.1460233C>T | NCBI36 |
| NG_011581.1:g.68992C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329066.9:c.1188C>T MANE Select | ENSP00000329869.4:p.Arg396= | |
| ENST00000329066.8:c.1188C>T | ENSP00000329869.4:p.Arg396= | |
| ENST00000345913.8:c.1188C>T | ENSP00000318820.7:p.Arg396= | |
| ENST00000346956.7:c.1188C>T | ENSP00000263886.6:p.Arg396= | |
| ENST00000382198.5:c.820-7142C>T | ENSP00000371633.1:n.820-7142C>T | |
| ENST00000382201.7:c.1188C>T | ENSP00000371636.3:p.Arg396= | |
| ENST00000422464.5:c.975C>T | ENSP00000405788.1:p.Arg325= | |
| ENST00000497517.6:n.181-7142C>T | ||
| NM_000547.5:c.1188C>T | NP_000538.3:p.Arg396= | |
| NM_001206744.1:c.1188C>T | NP_001193673.1:p.Arg396= | |
| NM_001206745.1:c.1188C>T | NP_001193674.1:p.Arg396= | |
| NM_175719.3:c.1188C>T | NP_783650.1:p.Arg396= | |
| NM_175721.3:c.1188C>T | NP_783652.1:p.Arg396= | |
| NM_175722.3:c.820-7142C>T | NP_783653.1:n.820-7142C>T | |
| XM_011510379.1:c.1188C>T | XP_011508681.1:p.Arg396= | |
| XM_011510380.1:c.1188C>T | XP_011508682.1:p.Arg396= | |
| XM_011510381.1:c.1188C>T | XP_011508683.1:p.Arg396= | |
| XM_011510382.1:c.1188C>T | XP_011508684.1:p.Arg396= | |
| XR_922681.1:n.1189C>T | ||
| XM_011510380.3:c.1224C>T | XP_011508682.2:p.Arg408= | |
| XM_024453085.1:c.1224C>T | XP_024308853.1:p.Arg408= | |
| XM_024453086.1:c.1224C>T | XP_024308854.1:p.Arg408= | |
| XM_024453087.1:c.1188C>T | XP_024308855.1:p.Arg396= | |
| XM_024453088.1:c.1188C>T | XP_024308856.1:p.Arg396= | |
| XM_024453089.1:c.1188C>T | XP_024308857.1:p.Arg396= | |
| XM_024453090.1:c.1224C>T | XP_024308858.1:p.Arg408= | |
| XM_024453091.1:c.1224C>T | XP_024308859.1:p.Arg408= | |
| XM_024453092.1:c.1224C>T | XP_024308860.1:p.Arg408= | |
| XM_024453093.1:c.856-7142C>T | XP_024308861.1:n.856-7142C>T | |
| NM_001206744.2:c.1188C>T MANE Select | NP_001193673.1:p.Arg396= | |
| NM_000547.6:c.1188C>T | NP_000538.3:p.Arg396= | |
| NM_001206745.2:c.1188C>T | NP_001193674.1:p.Arg396= | |
| NM_175719.4:c.1188C>T | NP_783650.1:p.Arg396= |