MyVariant.info:
GRCh37
chr6:g.31237774G>A
gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31269997G>A , CM000668.2:g.31269997G>A | GRCh38 |
| NC_000006.11:g.31237774G>A , CM000668.1:g.31237774G>A | GRCh37 |
| NC_000006.10:g.31345753G>A | NCBI36 |
| NG_029422.2:g.7135C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.984C>T MANE Select | ENSP00000365402.5:p.Val328= | |
| ENST00000376228.9:c.984C>T | ENSP00000365402.5:p.Val328= | |
| ENST00000376237.8:c.*571C>T | ENSP00000365412.4:n.*571C>T | |
| ENST00000383329.7:c.984C>T | ENSP00000372819.3:p.Val328= | |
| ENST00000470363.5:n.302C>T | ||
| ENST00000487245.5:n.1343C>T | ||
| NM_002117.5:c.984C>T | NP_002108.4:p.Val328= | |
| NM_002117.6:c.984C>T MANE Select | NP_002108.4:p.Val328= |