Linked Data
gnomAD v4:
6-31271163-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31271163C>G , CM000668.2:g.31271163C>G | GRCh38 |
| NC_000006.11:g.31238940C>G , CM000668.1:g.31238940C>G | GRCh37 |
| NC_000006.10:g.31346919C>G | NCBI36 |
| NG_029422.2:g.5969G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.529G>C MANE Select | ENSP00000365402.5:p.Ala177Pro | |
| ENST00000376228.9:c.529G>C | ENSP00000365402.5:p.Ala177Pro | |
| ENST00000376237.8:c.*116G>C | ENSP00000365412.4:n.*116G>C | |
| ENST00000383329.7:c.529G>C | ENSP00000372819.3:p.Ala177Pro | |
| ENST00000415537.1:c.527G>C | ||
| ENST00000484378.1:n.798G>C | ||
| ENST00000487245.5:n.888G>C | ||
| ENST00000495835.1:n.718G>C | ||
| NM_002117.5:c.529G>C | NP_002108.4:p.Ala177Pro | |
| NM_002117.6:c.529G>C MANE Select | NP_002108.4:p.Ala177Pro |