Linked Data
gnomAD v4:
14-31393938-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.31393938A>C , CM000676.2:g.31393938A>C | GRCh38 |
| NC_000014.8:g.31863144A>C , CM000676.1:g.31863144A>C | GRCh37 |
| NC_000014.7:g.30932895A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000543095.7:c.772+114T>G MANE Select | ENSP00000437968.2:n.772+114T>G | |
| ENST00000543095.6:c.772+114T>G | ENSP00000437968.2:n.772+114T>G | |
| ENST00000549185.5:c.*868+114T>G | ENSP00000446654.1:n.*868+114T>G | |
| NM_015473.3:c.772+114T>G | NP_056288.2:n.772+114T>G | |
| NM_015473.4:c.772+114T>G MANE Select | NP_056288.2:n.772+114T>G |