Linked Data
MyVariant Identifiers:
chr9:g.2729565C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.2729565C>G , CM000671.2:g.2729565C>G | GRCh38 |
| NC_000009.11:g.2729565C>G , CM000671.1:g.2729565C>G | GRCh37 |
| NC_000009.10:g.2719565C>G | NCBI36 |
| NG_012181.1:g.17040C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382082.4:c.1476C>G (KCNV2) MANE Select | ENSP00000371514.3:p.Leu492= | |
| ENST00000382082.3:c.1476C>G (KCNV2) | ENSP00000371514.3:p.Leu492= | |
| ENST00000490444.2:c.277-9033G>C (PUM3) | ENSP00000474467.1:n.277-9033G>C | |
| NM_133497.3:c.1476C>G (KCNV2) | NP_598004.1:p.Leu492= | |
| NM_133497.4:c.1476C>G (KCNV2) MANE Select | NP_598004.1:p.Leu492= |