Linked Data
ClinVar Variation Id:
2002012
ClinVar RCV Id:
RCV002820071
dbSNP Id:
rs2130869419
COSMIC:
COSM3656763
MyVariant Identifiers:
chr9:g.2729610G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.2729610G>A , CM000671.2:g.2729610G>A | GRCh38 |
| NC_000009.11:g.2729610G>A , CM000671.1:g.2729610G>A | GRCh37 |
| NC_000009.10:g.2719610G>A | NCBI36 |
| NG_012181.1:g.17085G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382082.4:c.1521G>A (KCNV2) MANE Select | ENSP00000371514.3:p.Glu507= | |
| ENST00000382082.3:c.1521G>A (KCNV2) | ENSP00000371514.3:p.Glu507= | |
| ENST00000490444.2:c.277-9078C>T (PUM3) | ENSP00000474467.1:n.277-9078C>T | |
| NM_133497.3:c.1521G>A (KCNV2) | NP_598004.1:p.Glu507= | |
| NM_133497.4:c.1521G>A (KCNV2) MANE Select | NP_598004.1:p.Glu507= |