Linked Data
ClinVar Variation Id:
795270
ClinVar RCV Id:
RCV001445396
dbSNP Id:
rs1599615180
MyVariant Identifiers:
chr19:g.13007169C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12896355C>A , CM000681.2:g.12896355C>A | GRCh38 |
| NC_000019.9:g.13007169C>A , CM000681.1:g.13007169C>A | GRCh37 |
| NC_000019.8:g.12868169C>A | NCBI36 |
| NG_009292.1:g.10196C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222214.10:c.786C>A MANE Select | ENSP00000222214.4:p.Gly262= | |
| ENST00000222214.9:c.786C>A | ENSP00000222214.4:p.Gly262= | |
| ENST00000421816.6:n.764C>A | ||
| ENST00000585420.5:n.1116C>A | ||
| ENST00000590530.5:c.*226C>A | ENSP00000468452.1:n.*226C>A | |
| ENST00000591043.1:n.822C>A | ||
| ENST00000591470.5:c.786C>A | ENSP00000466845.1:p.Gly262= | |
| NM_000159.3:c.786C>A | NP_000150.1:p.Gly262= | |
| NM_013976.3:c.786C>A | NP_039663.1:p.Gly262= | |
| NR_102316.1:n.949C>A | ||
| NR_102317.1:n.1167C>A | ||
| XM_006722721.2:c.786C>A | XP_006722784.1:p.Gly262= | |
| XM_011527899.1:c.786C>A | XP_011526201.1:p.Gly262= | |
| XM_011527900.1:c.786C>A | XP_011526202.1:p.Gly262= | |
| XM_011527899.2:c.786C>A | XP_011526201.1:p.Gly262= | |
| XM_011527900.2:c.786C>A | XP_011526202.1:p.Gly262= | |
| XM_017026580.1:c.786C>A | XP_016882069.1:p.Gly262= | |
| NM_000159.4:c.786C>A MANE Select | NP_000150.1:p.Gly262= | |
| NM_013976.4:c.786C>A | NP_039663.1:p.Gly262= | |
| NM_013976.5:c.786C>A | NP_039663.1:p.Gly262= |