Linked Data
gnomAD v4:
10-119651650-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119651650C>G , CM000672.2:g.119651650C>G | GRCh38 |
| NC_000010.10:g.121411162C>G , CM000672.1:g.121411162C>G | GRCh37 |
| NC_000010.9:g.121401152C>G | NCBI36 |
| NG_016125.1:g.5281C>G , LRG_742:g.5281C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000369085.8:c.-26C>G MANE Select | ENSP00000358081.4:n.-26C>G | |
| ENST00000369085.7:c.-26C>G | ENSP00000358081.3:n.-26C>G | |
| NM_004281.3:c.-26C>G , LRG_742t1:c.-26C>G | NP_004272.2:n.-26C>G | |
| XM_005270287.1:c.-26C>G | XP_005270344.1:n.-26C>G | |
| XM_005270287.2:c.-26C>G | XP_005270344.1:n.-26C>G | |
| NM_004281.4:c.-26C>G MANE Select | NP_004272.2:n.-26C>G |