Linked Data
gnomAD v4:
5-97015082-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.97015082C>A , CM000667.2:g.97015082C>A | GRCh38 |
| NC_000005.9:g.96350786C>A , CM000667.1:g.96350786C>A | GRCh37 |
| NC_000005.8:g.96376542C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000231368.10:c.2363C>A MANE Select | ENSP00000231368.5:p.Ala788Asp | |
| ENST00000231368.9:c.2363C>A | ENSP00000231368.5:p.Ala788Asp | |
| ENST00000395770.3:c.2321C>A | ENSP00000379117.3:p.Ala774Asp | |
| NM_005575.2:c.2363C>A | NP_005566.2:p.Ala788Asp | |
| NM_175920.3:c.2321C>A | NP_787116.2:p.Ala774Asp | |
| XM_024446045.1:c.2363C>A | XP_024301813.1:p.Ala788Asp | |
| NM_005575.3:c.2363C>A MANE Select | NP_005566.2:p.Ala788Asp | |
| NM_175920.4:c.2321C>A | NP_787116.2:p.Ala774Asp |