Linked Data
gnomAD v4:
10-26697698-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.26697698T>A , CM000672.2:g.26697698T>A | GRCh38 |
| NC_000010.10:g.26986627T>A , CM000672.1:g.26986627T>A | GRCh37 |
| NC_000010.9:g.27026633T>A | NCBI36 |
| NG_008972.1:g.5033T>A | |
| NG_008972.2:g.5033T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376215.9:c.-14T>A | ENSP00000365388.5:n.-14T>A | |
| NM_014317.3:c.-14T>A | NP_055132.2:n.-14T>A | |
| XR_428636.2:n.275T>A | ||
| XR_930486.1:n.275T>A | ||
| NM_001321978.1:c.-14T>A | NP_001308907.1:n.-14T>A | |
| NM_001321979.1:c.-607T>A | NP_001308908.1:n.-607T>A | |
| NM_014317.4:c.-14T>A | NP_055132.2:n.-14T>A | |
| XM_024447922.1:c.-14T>A | XP_024303690.1:n.-14T>A | |
| XR_428636.4:n.275T>A |