Linked Data
dbSNP Id:
rs8176751
gnomAD v3:
9-133255635-C-G
gnomAD v4:
9-133255635-C-G
MyVariant Identifiers:
chr9:g.136131022C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133255635C>G , CM000671.2:g.133255635C>G | GRCh38 |
| NC_000009.11:g.136131022C>G , CM000671.1:g.136131022C>G | GRCh37 |
| NC_000009.10:g.135120843C>G | NCBI36 |
| NG_006669.1:g.22033G>C | |
| NG_006669.2:g.24581G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.1125G>C | ||
| ENST00000647353.1:n.54-4483G>C | ||
| ENST00000679909.1:c.28+19527G>C | ENSP00000506089.1:n.28+19527G>C | |
| ENST00000453660.3:n.1107G>C | ||
| ENST00000538324.2:c.1089G>C | ENSP00000483018.1:p.Pro363= | |
| ENST00000611156.4:c.*31G>C | ENSP00000483265.1:n.*31G>C | |
| NM_020469.2:c.*31G>C | NP_065202.2:n.*31G>C | |
| NM_020469.3:c.*31G>C | NP_065202.2:n.*31G>C |