Linked Data
ClinVar Variation Id:
2565868
ClinVar RCV Id:
RCV003302093
dbSNP Id:
rs1663028563
gnomAD v3:
2-21002889-A-C
gnomAD v4:
2-21002889-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21002889A>C , CM000664.2:g.21002889A>C | GRCh38 |
| NC_000002.11:g.21225761A>C , CM000664.1:g.21225761A>C | GRCh37 |
| NC_000002.10:g.21079266A>C | NCBI36 |
| NG_011793.1:g.46185T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233242.5:c.12533T>G MANE Select | ENSP00000233242.1:p.Val4178Gly | |
| ENST00000616098.4:c.12533T>G | ENSP00000477990.1:p.Val4178Gly | |
| NM_000384.2:c.12533T>G | NP_000375.2:p.Val4178Gly | |
| XM_011532809.1:c.5870-3616T>G | XP_011531111.1:n.5870-3616T>G | |
| NM_000384.3:c.12533T>G MANE Select | NP_000375.3:p.Val4178Gly |