Linked Data
ClinVar Variation Id:
242224
ClinVar RCV Id:
RCV000503916
RCV001154529
RCV001151517
RCV001151518
RCV002418033
RCV002518373
RCV003437032
dbSNP Id:
rs765264494
ExAC:
5:1279409 G / C
gnomAD v2:
5-1279409-G-C
gnomAD v3:
5-1279294-G-C
gnomAD v4:
5-1279294-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1279294G>C , CM000667.2:g.1279294G>C | GRCh38 |
| NC_000005.9:g.1279409G>C , CM000667.1:g.1279409G>C | GRCh37 |
| NC_000005.8:g.1332409G>C | NCBI36 |
| NG_009265.1:g.20754C>G , LRG_343:g.20754C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310581.10:c.2127C>G MANE Select | ENSP00000309572.5:p.Val709= | |
| ENST00000656021.1:c.*1673C>G | ENSP00000499759.1:n.*1673C>G | |
| ENST00000310581.9:c.2127C>G | ENSP00000309572.5:p.Val709= | |
| ENST00000334602.10:c.2127C>G | ENSP00000334346.6:p.Val709= | |
| ENST00000460137.6:c.2127C>G | ENSP00000425003.1:p.Val709= | |
| ENST00000484238.6:n.940C>G | ||
| ENST00000508104.2:c.2127C>G | ENSP00000426042.2:p.Val709= | |
| NM_001193376.1:c.2127C>G | NP_001180305.1:p.Val709= | |
| NM_198253.2:c.2127C>G , LRG_343t1:c.2127C>G | NP_937983.2:p.Val709= | |
| XM_011514104.1:c.597C>G | XP_011512406.1:p.Val199= | |
| XM_011514105.1:c.483C>G | XP_011512407.1:p.Val161= | |
| XM_011514106.1:c.483C>G | XP_011512408.1:p.Val161= | |
| NR_149162.1:n.2185C>G | ||
| NR_149163.1:n.2185C>G | ||
| NM_001193376.2:c.2127C>G | NP_001180305.1:p.Val709= | |
| NM_198253.3:c.2127C>G MANE Select | NP_937983.2:p.Val709= | |
| NR_149162.2:n.2206C>G | ||
| NR_149163.2:n.2206C>G | ||
| NM_001193376.3:c.2127C>G | NP_001180305.1:p.Val709= | |
| NR_149162.3:n.2206C>G | ||
| NR_149163.3:n.2206C>G |