Linked Data
gnomAD v4:
10-119651649-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119651649G>C , CM000672.2:g.119651649G>C | GRCh38 |
| NC_000010.10:g.121411161G>C , CM000672.1:g.121411161G>C | GRCh37 |
| NC_000010.9:g.121401151G>C | NCBI36 |
| NG_016125.1:g.5280G>C , LRG_742:g.5280G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000369085.8:c.-27G>C MANE Select | ENSP00000358081.4:n.-27G>C | |
| ENST00000369085.7:c.-27G>C | ENSP00000358081.3:n.-27G>C | |
| NM_004281.3:c.-27G>C , LRG_742t1:c.-27G>C | NP_004272.2:n.-27G>C | |
| XM_005270287.1:c.-27G>C | XP_005270344.1:n.-27G>C | |
| XM_005270287.2:c.-27G>C | XP_005270344.1:n.-27G>C | |
| NM_004281.4:c.-27G>C MANE Select | NP_004272.2:n.-27G>C |