Linked Data
ClinVar Variation Id:
953257
ClinVar RCV Id:
RCV002241416
dbSNP Id:
rs933589600
gnomAD v4:
2-189050638-C-A
MyVariant Identifiers:
chr2:g.189915364C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189050638C>A , CM000664.2:g.189050638C>A | GRCh38 |
| NC_000002.11:g.189915364C>A , CM000664.1:g.189915364C>A | GRCh37 |
| NC_000002.10:g.189623609C>A | NCBI36 |
| NG_011799.1:g.134242G>T | |
| NG_011799.2:g.134242G>T | |
| NG_011799.3:g.179664G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374866.9:c.2970G>T MANE Select | ENSP00000364000.3:p.Gly990= | |
| ENST00000374866.7:c.2970G>T | ENSP00000364000.3:p.Gly990= | |
| ENST00000618828.1:c.1809G>T | ENSP00000482184.1:p.Gly603= | |
| NM_000393.3:c.2970G>T | NP_000384.2:p.Gly990= | |
| XM_011510573.1:c.2832G>T | XP_011508875.1:p.Gly944= | |
| NM_000393.4:c.2970G>T | NP_000384.2:p.Gly990= | |
| XM_011510573.3:c.2832G>T | XP_011508875.1:p.Gly944= | |
| NM_000393.5:c.2970G>T MANE Select | NP_000384.2:p.Gly990= |