Linked Data
gnomAD v4:
17-44372234-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44372234T>C , CM000679.2:g.44372234T>C | GRCh38 |
| NC_000017.10:g.42449602T>C , CM000679.1:g.42449602T>C | GRCh37 |
| NC_000017.9:g.39805128T>C | NCBI36 |
| NG_008331.1:g.22272A>G , LRG_479:g.22272A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262407.6:c.*130A>G MANE Select | ENSP00000262407.5:n.*130A>G | |
| ENST00000648408.1:c.2564A>G | ||
| ENST00000262407.5:c.*130A>G | ENSP00000262407.5:n.*130A>G | |
| ENST00000587295.5:c.443A>G | ||
| ENST00000588098.1:c.227A>G | ||
| NM_000419.3:c.*130A>G , LRG_479t1:c.*130A>G | NP_000410.2:n.*130A>G | |
| XM_011524749.1:c.*130A>G | XP_011523051.1:n.*130A>G | |
| XM_011524750.1:c.*130A>G | XP_011523052.1:n.*130A>G | |
| NM_000419.4:c.*130A>G | NP_000410.2:n.*130A>G | |
| NM_000419.5:c.*130A>G MANE Select | NP_000410.2:n.*130A>G |