Linked Data
gnomAD v4:
8-10612777-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.10612777C>A , CM000670.2:g.10612777C>A | GRCh38 |
| NC_000008.10:g.10470287C>A , CM000670.1:g.10470287C>A | GRCh37 |
| NC_000008.9:g.10507697C>A | NCBI36 |
| NG_028035.1:g.47331G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382483.4:c.1321G>T MANE Select | ENSP00000371923.3:p.Gly441Trp | |
| ENST00000382483.3:c.1321G>T | ENSP00000371923.3:p.Gly441Trp | |
| NM_178857.5:c.1321G>T | NP_849188.4:p.Gly441Trp | |
| NM_178857.6:c.1321G>T MANE Select | NP_849188.4:p.Gly441Trp |