Linked Data
ClinVar Variation Id:
2098303
ClinVar RCV Id:
RCV003030878
dbSNP Id:
rs1763560355
MyVariant Identifiers:
chr5:g.89913641T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.90617824T>G , CM000667.2:g.90617824T>G | GRCh38 |
| NC_000005.9:g.89913641T>G , CM000667.1:g.89913641T>G | GRCh37 |
| NC_000005.8:g.89949397T>G | NCBI36 |
| NG_007083.1:g.64025T>G | |
| NG_007083.2:g.93481T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000405460.9:c.228T>G MANE Select | ENSP00000384582.2:p.Gly76= | |
| ENST00000638316.1:n.438T>G | ||
| ENST00000638638.1:n.635T>G | ||
| ENST00000640109.1:n.324T>G | ||
| ENST00000640281.1:n.287T>G | ||
| ENST00000405460.6:c.228T>G | ENSP00000384582.2:p.Gly76= | |
| ENST00000508842.5:c.240T>G | ENSP00000425936.1:p.Gly80= | |
| NM_032119.3:c.228T>G | NP_115495.3:p.Gly76= | |
| NR_003149.1:n.324T>G | ||
| XM_011543675.1:c.228T>G | XP_011541977.1:p.Gly76= | |
| XM_011543676.1:c.228T>G | XP_011541978.1:p.Gly76= | |
| XM_011543678.1:c.228T>G | XP_011541980.1:p.Gly76= | |
| XM_011543679.1:c.228T>G | XP_011541981.1:p.Gly76= | |
| NM_032119.4:c.228T>G MANE Select | NP_115495.3:p.Gly76= | |
| XM_017009963.2:c.228T>G | XP_016865452.1:p.Gly76= | |
| XM_017009964.2:c.228T>G | XP_016865453.1:p.Gly76= | |
| XM_017009965.1:c.225T>G | XP_016865454.1:p.Gly75= | |
| XM_017009966.2:c.228T>G | XP_016865455.1:p.Gly76= | |
| XM_017009967.1:c.228T>G | XP_016865456.1:p.Gly76= | |
| XM_017009968.2:c.228T>G | XP_016865457.1:p.Gly76= | |
| XM_017009969.2:c.228T>G | XP_016865458.1:p.Gly76= | |
| XM_017009970.2:c.228T>G | XP_016865459.1:p.Gly76= | |
| XM_017009971.2:c.228T>G | XP_016865460.1:p.Gly76= | |
| XM_017009974.2:c.228T>G | XP_016865463.1:p.Gly76= | |
| NR_003149.2:n.327T>G |