Linked Data
ClinVar Variation Id:
1097131
ClinVar RCV Id:
RCV001418602
dbSNP Id:
rs2118362315
MyVariant Identifiers:
chr9:g.104192130C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.101429848C>A , CM000671.2:g.101429848C>A | GRCh38 |
| NC_000009.11:g.104192130C>A , CM000671.1:g.104192130C>A | GRCh37 |
| NC_000009.10:g.103231951C>A | NCBI36 |
| NG_012387.1:g.10933G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647789.2:c.231G>T MANE Select | ENSP00000497767.1:p.Val77= | |
| ENST00000648064.1:c.231G>T | ENSP00000497990.1:p.Val77= | |
| ENST00000648758.1:c.231G>T | ENSP00000497731.1:p.Val77= | |
| ENST00000648906.1:n.401G>T | ||
| ENST00000649902.1:c.231G>T | ENSP00000497216.1:p.Val77= | |
| ENST00000650613.1:n.307G>T | ||
| ENST00000374855.8:c.231G>T | ENSP00000363988.4:p.Val77= | |
| ENST00000468981.3:n.28G>T | ||
| ENST00000616752.1:c.231G>T | ENSP00000481363.1:p.Val77= | |
| NM_000035.3:c.231G>T | NP_000026.2:p.Val77= | |
| NM_000035.4:c.231G>T MANE Select | NP_000026.2:p.Val77= |