Linked Data
gnomAD v4:
17-44372229-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44372229T>C , CM000679.2:g.44372229T>C | GRCh38 |
| NC_000017.10:g.42449597T>C , CM000679.1:g.42449597T>C | GRCh37 |
| NC_000017.9:g.39805123T>C | NCBI36 |
| NG_008331.1:g.22277A>G , LRG_479:g.22277A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262407.6:c.*135A>G MANE Select | ENSP00000262407.5:n.*135A>G | |
| ENST00000648408.1:c.2569A>G | ||
| ENST00000262407.5:c.*135A>G | ENSP00000262407.5:n.*135A>G | |
| ENST00000587295.5:c.448A>G | ||
| ENST00000588098.1:c.232A>G | ||
| NM_000419.3:c.*135A>G , LRG_479t1:c.*135A>G | NP_000410.2:n.*135A>G | |
| XM_011524749.1:c.*135A>G | XP_011523051.1:n.*135A>G | |
| XM_011524750.1:c.*135A>G | XP_011523052.1:n.*135A>G | |
| NM_000419.4:c.*135A>G | NP_000410.2:n.*135A>G | |
| NM_000419.5:c.*135A>G MANE Select | NP_000410.2:n.*135A>G |