Linked Data
ClinVar Variation Id:
1943536
ClinVar RCV Id:
RCV002650500
dbSNP Id:
rs1555455539
MyVariant Identifiers:
chr16:g.10031863G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.9938006G>A , CM000678.2:g.9938006G>A | GRCh38 |
| NC_000016.9:g.10031863G>A , CM000678.1:g.10031863G>A | GRCh37 |
| NC_000016.8:g.9939364G>A | NCBI36 |
| NG_011812.1:g.249749C>T | |
| NG_011812.2:g.249749C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330684.4:c.960C>T MANE Select | ENSP00000332549.3:p.Cys320= | |
| ENST00000535259.6:c.489C>T | ENSP00000441572.3:p.Cys163= | |
| ENST00000636273.2:n.553C>T | ||
| ENST00000637393.1:c.552C>T | ENSP00000490232.1:p.Cys184= | |
| ENST00000674742.1:c.489C>T | ENSP00000502200.1:p.Cys163= | |
| ENST00000675189.1:n.1444C>T | ||
| ENST00000675398.1:c.960C>T | ENSP00000502752.1:p.Cys320= | |
| ENST00000330684.3:c.960C>T | ENSP00000332549.3:p.Cys320= | |
| ENST00000396573.6:c.960C>T | ENSP00000379818.2:p.Cys320= | |
| ENST00000396575.6:c.549C>T | ENSP00000379820.3:p.Cys183= | |
| ENST00000461292.3:n.599C>T | ||
| ENST00000535259.5:c.549C>T | ENSP00000441572.2:p.Cys183= | |
| ENST00000562109.5:c.960C>T | ENSP00000454998.1:p.Cys320= | |
| ENST00000566683.1:n.241-46906C>T | ||
| ENST00000568247.3:n.852C>T | ||
| NM_000833.4:c.960C>T | NP_000824.1:p.Cys320= | |
| NM_001134407.2:c.960C>T | NP_001127879.1:p.Cys320= | |
| NM_001134408.2:c.960C>T | NP_001127880.1:p.Cys320= | |
| XM_011522456.1:c.801C>T | XP_011520758.1:p.Cys267= | |
| XM_011522457.1:c.702C>T | XP_011520759.1:p.Cys234= | |
| XM_011522458.1:c.489C>T | XP_011520760.1:p.Cys163= | |
| XM_011522459.1:c.489C>T | XP_011520761.1:p.Cys163= | |
| XM_011522460.1:c.489C>T | XP_011520762.1:p.Cys163= | |
| XM_011522461.1:c.960C>T | XP_011520763.1:p.Cys320= | |
| XM_011522458.3:c.489C>T | XP_011520760.1:p.Cys163= | |
| XM_011522461.3:c.960C>T | XP_011520763.1:p.Cys320= | |
| XM_017023172.1:c.1116C>T | XP_016878661.1:p.Cys372= | |
| XM_017023173.1:c.1116C>T | XP_016878662.1:p.Cys372= | |
| NM_001134407.3:c.960C>T MANE Select | NP_001127879.1:p.Cys320= | |
| NM_000833.5:c.960C>T | NP_000824.1:p.Cys320= |