Linked Data
gnomAD v4:
4-186191698-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186191698C>A , CM000666.2:g.186191698C>A | GRCh38 |
| NC_000004.11:g.187112852C>A , CM000666.1:g.187112852C>A | GRCh37 |
| NC_000004.10:g.187349846C>A | NCBI36 |
| NG_007965.1:g.5179C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378802.5:c.-126C>A MANE Select | ENSP00000368079.4:n.-126C>A | |
| ENST00000378802.4:c.-126C>A | ENSP00000368079.4:n.-126C>A | |
| NM_207352.3:c.-126C>A | NP_997235.3:n.-126C>A | |
| XM_005262935.2:c.-126C>A | XP_005262992.1:n.-126C>A | |
| XM_017008037.1:c.-436C>A | XP_016863526.1:n.-436C>A | |
| NM_207352.4:c.-126C>A MANE Select | NP_997235.3:n.-126C>A |