Linked Data
MyVariant Identifiers:
chr9:g.2729523T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.2729523T>A , CM000671.2:g.2729523T>A | GRCh38 |
| NC_000009.11:g.2729523T>A , CM000671.1:g.2729523T>A | GRCh37 |
| NC_000009.10:g.2719523T>A | NCBI36 |
| NG_012181.1:g.16998T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382082.4:c.1434T>A (KCNV2) MANE Select | ENSP00000371514.3:p.Ile478= | |
| ENST00000382082.3:c.1434T>A (KCNV2) | ENSP00000371514.3:p.Ile478= | |
| ENST00000490444.2:c.277-8991A>T (PUM3) | ENSP00000474467.1:n.277-8991A>T | |
| NM_133497.3:c.1434T>A (KCNV2) | NP_598004.1:p.Ile478= | |
| NM_133497.4:c.1434T>A (KCNV2) MANE Select | NP_598004.1:p.Ile478= |