Linked Data
gnomAD v4:
6-108561764-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.108561764T>G , CM000668.2:g.108561764T>G | GRCh38 |
| NC_000006.11:g.108882967T>G , CM000668.1:g.108882967T>G | GRCh37 |
| NC_000006.10:g.108989660T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000406360.2:c.556T>G MANE Select | ENSP00000385824.1:p.Trp186Gly | |
| ENST00000343882.10:c.556T>G | ENSP00000339527.6:p.Trp186Gly | |
| ENST00000406360.1:c.556T>G | ENSP00000385824.1:p.Trp186Gly | |
| NM_001455.3:c.556T>G | NP_001446.1:p.Trp186Gly | |
| NM_201559.2:c.556T>G | NP_963853.1:p.Trp186Gly | |
| XM_005266867.3:c.-129T>G | XP_005266924.1:n.-129T>G | |
| XM_005266867.4:c.-129T>G | XP_005266924.1:n.-129T>G | |
| NM_001455.4:c.556T>G MANE Select | NP_001446.1:p.Trp186Gly | |
| NM_201559.3:c.556T>G | NP_963853.1:p.Trp186Gly |