Linked Data
ClinVar Variation Id:
1648633
ClinVar RCV Id:
RCV002160897
dbSNP Id:
rs1881793401
MyVariant Identifiers:
chr14:g.29236890G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.28767684G>A , CM000676.2:g.28767684G>A | GRCh38 |
| NC_000014.8:g.29236890G>A , CM000676.1:g.29236890G>A | GRCh37 |
| NC_000014.7:g.28306641G>A | NCBI36 |
| NG_009367.1:g.5604G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706482.1:c.405G>A | ENSP00000516406.1:p.Gly135= | |
| ENST00000313071.7:c.405G>A MANE Select | ENSP00000339004.3:p.Gly135= | |
| ENST00000313071.6:c.405G>A | ENSP00000339004.3:p.Gly135= | |
| NM_005249.4:c.405G>A | NP_005240.3:p.Gly135= | |
| NM_005249.5:c.405G>A MANE Select | NP_005240.3:p.Gly135= |