Linked Data
dbSNP Id:
rs1450235074
gnomAD v3:
9-133274220-T-C
gnomAD v4:
9-133274220-T-C
MyVariant Identifiers:
chr9:g.133274220T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133274220T>C , CM000671.2:g.133274220T>C | GRCh38 |
| NC_000009.11:g.136149636T>C , CM000671.1:g.136149636T>C | GRCh37 |
| NC_000009.10:g.135139457T>C | NCBI36 |
| NG_006669.1:g.3415A>G | |
| NG_006669.2:g.5995A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000453660.4:n.58+942A>G | ||
| ENST00000647353.1:n.53+942A>G | ||
| ENST00000651471.1:n.63+1742A>G | ||
| ENST00000679909.1:c.28+942A>G | ENSP00000506089.1:n.28+942A>G | |
| ENST00000453660.3:n.40+942A>G | ||
| ENST00000538324.2:c.28+942A>G | ENSP00000483018.1:n.28+942A>G | |
| ENST00000611156.4:c.28+942A>G | ENSP00000483265.1:n.28+942A>G | |
| NM_020469.2:c.28+942A>G | NP_065202.2:n.28+942A>G | |
| NM_020469.3:c.28+942A>G | NP_065202.2:n.28+942A>G |