Linked Data
gnomAD v4:
20-10644929-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10644929C>A , CM000682.2:g.10644929C>A | GRCh38 |
| NC_000020.10:g.10625577C>A , CM000682.1:g.10625577C>A | GRCh37 |
| NC_000020.9:g.10573577C>A | NCBI36 |
| NG_007496.1:g.34118G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.2278G>T MANE Select | ENSP00000254958.4:p.Val760Leu | |
| ENST00000617965.2:n.2867G>T | ||
| ENST00000254958.9:c.2278G>T | ENSP00000254958.4:p.Val760Leu | |
| ENST00000423891.6:n.2144G>T | ||
| ENST00000488480.2:n.675G>T | ||
| NM_000214.2:c.2278G>T | NP_000205.1:p.Val760Leu | |
| NM_000214.3:c.2278G>T MANE Select | NP_000205.1:p.Val760Leu |