Linked Data
gnomAD v4:
10-119651427-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119651427T>G , CM000672.2:g.119651427T>G | GRCh38 |
| NC_000010.10:g.121410939T>G , CM000672.1:g.121410939T>G | GRCh37 |
| NC_000010.9:g.121400929T>G | NCBI36 |
| NG_016125.1:g.5058T>G , LRG_742:g.5058T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369085.8:c.-249T>G MANE Select | ENSP00000358081.4:n.-249T>G | |
| ENST00000369085.7:c.-249T>G | ENSP00000358081.3:n.-249T>G | |
| NM_004281.3:c.-249T>G , LRG_742t1:c.-249T>G | NP_004272.2:n.-249T>G | |
| XM_005270287.1:c.-249T>G | XP_005270344.1:n.-249T>G | |
| XM_005270287.2:c.-249T>G | XP_005270344.1:n.-249T>G | |
| NM_004281.4:c.-249T>G MANE Select | NP_004272.2:n.-249T>G |