Linked Data
dbSNP Id:
rs765352854
ExAC:
4:100239331 A / G
gnomAD v2:
4-100239331-A-G
gnomAD v3:
4-99318174-A-G
gnomAD v4:
4-99318174-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99318174A>G , CM000666.2:g.99318174A>G | GRCh38 |
| NC_000004.11:g.100239331A>G , CM000666.1:g.100239331A>G | GRCh37 |
| NC_000004.10:g.100458354A>G | NCBI36 |
| NG_011435.1:g.8242T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305046.13:c.131T>C MANE Select | ENSP00000306606.8:p.Val44Ala | |
| ENST00000639454.1:c.131T>C | ENSP00000491622.1:p.Val44Ala | |
| ENST00000305046.12:c.131T>C | ENSP00000306606.8:p.Val44Ala | |
| ENST00000504498.1:n.185T>C | ||
| ENST00000506651.5:c.11T>C | ENSP00000425998.2:p.Val4Ala | |
| ENST00000515694.4:n.2226T>C | ||
| ENST00000625860.2:c.11T>C | ENSP00000486614.1:p.Val4Ala | |
| ENST00000632775.1:n.694T>C | ||
| NM_000668.5:c.131T>C | NP_000659.2:p.Val44Ala | |
| NM_001286650.1:c.11T>C | NP_001273579.1:p.Val4Ala | |
| NM_000668.6:c.131T>C MANE Select | NP_000659.2:p.Val44Ala | |
| NM_001286650.2:c.11T>C | NP_001273579.1:p.Val4Ala |