Linked Data
ClinVar Variation Id:
1962865
ClinVar RCV Id:
RCV002735222
dbSNP Id:
rs1446409832
gnomAD v2:
11-5246995-A-G
gnomAD v4:
11-5225765-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5225765A>G , CM000673.2:g.5225765A>G | GRCh38 |
| NC_000011.9:g.5246995A>G , CM000673.1:g.5246995A>G | GRCh37 |
| NC_000011.8:g.5203571A>G | NCBI36 |
| NG_000007.3:g.71851T>C | |
| NG_059281.1:g.6307T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.316-39T>C | ENSP00000494175.1:n.316-39T>C | |
| ENST00000335295.4:c.316-39T>C MANE Select | ENSP00000333994.3:n.316-39T>C | |
| ENST00000475226.1:n.248-39T>C | ||
| ENST00000633227.1:c.*132-39T>C | ENSP00000488004.1:n.*132-39T>C | |
| NM_000518.4:c.316-39T>C | NP_000509.1:n.316-39T>C | |
| NM_000518.5:c.316-39T>C MANE Select | NP_000509.1:n.316-39T>C |