Linked Data
dbSNP Id:
rs1438600839
gnomAD v3:
9-130205068-C-T
gnomAD v4:
9-130205068-C-T
MyVariant Identifiers:
chr9:g.130205068C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.130205068C>T , CM000671.2:g.130205068C>T | GRCh38 |
| NC_000009.11:g.132967347C>T , CM000671.1:g.132967347C>T | GRCh37 |
| NC_000009.10:g.132007168C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372398.6:c.89+4086C>T MANE Select | ENSP00000361475.3:n.89+4086C>T | |
| ENST00000372398.5:c.89+4086C>T | ENSP00000361475.3:n.89+4086C>T | |
| ENST00000493042.1:n.143+4086C>T | ||
| ENST00000630865.1:c.35+4086C>T | ENSP00000486695.1:n.35+4086C>T | |
| NM_001128826.1:c.35+4086C>T | NP_001122298.1:n.35+4086C>T | |
| NM_014286.3:c.89+4086C>T | NP_055101.2:n.89+4086C>T | |
| NM_014286.4:c.89+4086C>T MANE Select | NP_055101.2:n.89+4086C>T | |
| NM_001128826.2:c.35+4086C>T | NP_001122298.1:n.35+4086C>T |