Linked Data
ClinVar Variation Id:
1151282
ClinVar RCV Id:
RCV001492136
dbSNP Id:
rs2141631974
COSMIC:
COSM3505668
MyVariant Identifiers:
chr16:g.10032214C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.9938357C>T , CM000678.2:g.9938357C>T | GRCh38 |
| NC_000016.9:g.10032214C>T , CM000678.1:g.10032214C>T | GRCh37 |
| NC_000016.8:g.9939715C>T | NCBI36 |
| NG_011812.1:g.249398G>A | |
| NG_011812.2:g.249398G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330684.4:c.609G>A MANE Select | ENSP00000332549.3:p.Val203= | |
| ENST00000535259.6:c.138G>A | ENSP00000441572.3:p.Val46= | |
| ENST00000636273.2:n.202G>A | ||
| ENST00000637393.1:c.201G>A | ENSP00000490232.1:p.Val67= | |
| ENST00000674742.1:c.138G>A | ENSP00000502200.1:p.Val46= | |
| ENST00000675189.1:n.1093G>A | ||
| ENST00000675398.1:c.609G>A | ENSP00000502752.1:p.Val203= | |
| ENST00000330684.3:c.609G>A | ENSP00000332549.3:p.Val203= | |
| ENST00000396573.6:c.609G>A | ENSP00000379818.2:p.Val203= | |
| ENST00000396575.6:c.198G>A | ENSP00000379820.3:p.Val66= | |
| ENST00000461292.3:n.248G>A | ||
| ENST00000535259.5:c.198G>A | ENSP00000441572.2:p.Val66= | |
| ENST00000562109.5:c.609G>A | ENSP00000454998.1:p.Val203= | |
| ENST00000566670.2:n.451G>A | ||
| ENST00000566683.1:n.241-47257G>A | ||
| ENST00000568247.3:n.501G>A | ||
| NM_000833.4:c.609G>A | NP_000824.1:p.Val203= | |
| NM_001134407.2:c.609G>A | NP_001127879.1:p.Val203= | |
| NM_001134408.2:c.609G>A | NP_001127880.1:p.Val203= | |
| XM_011522456.1:c.450G>A | XP_011520758.1:p.Val150= | |
| XM_011522457.1:c.351G>A | XP_011520759.1:p.Val117= | |
| XM_011522458.1:c.138G>A | XP_011520760.1:p.Val46= | |
| XM_011522459.1:c.138G>A | XP_011520761.1:p.Val46= | |
| XM_011522460.1:c.138G>A | XP_011520762.1:p.Val46= | |
| XM_011522461.1:c.609G>A | XP_011520763.1:p.Val203= | |
| XM_011522458.3:c.138G>A | XP_011520760.1:p.Val46= | |
| XM_011522461.3:c.609G>A | XP_011520763.1:p.Val203= | |
| XM_017023172.1:c.765G>A | XP_016878661.1:p.Val255= | |
| XM_017023173.1:c.765G>A | XP_016878662.1:p.Val255= | |
| NM_001134407.3:c.609G>A MANE Select | NP_001127879.1:p.Val203= | |
| NM_000833.5:c.609G>A | NP_000824.1:p.Val203= |