Linked Data
ClinVar Variation Id:
1479593
ClinVar RCV Id:
RCV001990989
dbSNP Id:
rs138850232
ExAC:
2:21229626 A / C
gnomAD v2:
2-21229626-A-C
gnomAD v3:
2-21006754-A-C
gnomAD v4:
2-21006754-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21006754A>C , CM000664.2:g.21006754A>C | GRCh38 |
| NC_000002.11:g.21229626A>C , CM000664.1:g.21229626A>C | GRCh37 |
| NC_000002.10:g.21083131A>C | NCBI36 |
| NG_011793.1:g.42320T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233242.5:c.10114T>G MANE Select | ENSP00000233242.1:p.Ser3372Ala | |
| ENST00000616098.4:c.10114T>G | ENSP00000477990.1:p.Ser3372Ala | |
| NM_000384.2:c.10114T>G | NP_000375.2:p.Ser3372Ala | |
| XM_011532809.1:c.5869+3979T>G | XP_011531111.1:n.5869+3979T>G | |
| NM_000384.3:c.10114T>G MANE Select | NP_000375.3:p.Ser3372Ala |