Linked Data
gnomAD v4:
20-57562966-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.57562966T>G , CM000682.2:g.57562966T>G | GRCh38 |
| NC_000020.10:g.56138022T>G , CM000682.1:g.56138022T>G | GRCh37 |
| NC_000020.9:g.55571428T>G | NCBI36 |
| NG_008205.1:g.6886T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319441.6:c.611-62T>G MANE Select | ENSP00000319814.4:n.611-62T>G | |
| ENST00000319441.5:c.611-62T>G | ENSP00000319814.4:n.611-62T>G | |
| ENST00000467047.1:n.1887T>G | ||
| ENST00000470051.1:n.133T>G | ||
| ENST00000498194.1:n.553-62T>G | ||
| NM_002591.3:c.611-62T>G | NP_002582.3:n.611-62T>G | |
| XM_011528839.1:c.215-62T>G | XP_011527141.1:n.215-62T>G | |
| XM_024451888.1:c.215-62T>G | XP_024307656.1:n.215-62T>G | |
| NM_002591.4:c.611-62T>G MANE Select | NP_002582.3:n.611-62T>G |