Linked Data
dbSNP Id:
rs1056629
gnomAD v2:
16-82182104-T-C
gnomAD v3:
16-82148499-T-C
gnomAD v4:
16-82148499-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.82148499T>C , CM000678.2:g.82148499T>C | GRCh38 |
| NC_000016.9:g.82182104T>C , CM000678.1:g.82182104T>C | GRCh37 |
| NC_000016.8:g.80739605T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000258169.9:c.*232A>G MANE Select | ENSP00000258169.4:n.*232A>G | |
| ENST00000258169.8:c.*232A>G | ENSP00000258169.4:n.*232A>G | |
| ENST00000563100.5:c.*72+160A>G | ENSP00000454996.1:n.*72+160A>G | |
| NM_005792.2:c.*232A>G MANE Select | NP_005783.2:n.*232A>G | |
| XM_011522808.1:c.*232A>G | XP_011521110.1:n.*232A>G | |
| XM_011522808.3:c.*232A>G | XP_011521110.1:n.*232A>G |