Linked Data
gnomAD v4:
1-229431545-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.229431545T>G , CM000663.2:g.229431545T>G | GRCh38 |
| NC_000001.10:g.229567292T>G , CM000663.1:g.229567292T>G | GRCh37 |
| NC_000001.9:g.227633915T>G | NCBI36 |
| NG_006672.1:g.7552A>C , LRG_429:g.7552A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000366683.4:c.1010A>C | ENSP00000355644.4:p.Glu337Ala | |
| ENST00000684723.1:c.953A>C | ENSP00000508084.1:p.Glu318Ala | |
| ENST00000366683.3:c.719A>C | ENSP00000355644.3:p.Glu240Ala | |
| ENST00000366684.7:c.1088A>C MANE Select | ENSP00000355645.3:p.Glu363Ala | |
| NM_001100.3:c.1088A>C , LRG_429t1:c.1088A>C | NP_001091.1:p.Glu363Ala | |
| NM_001100.4:c.1088A>C MANE Select | NP_001091.1:p.Glu363Ala |