Linked Data
gnomAD v4:
14-23393701-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23393701T>C , CM000676.2:g.23393701T>C | GRCh38 |
| NC_000014.8:g.23862910T>C , CM000676.1:g.23862910T>C | GRCh37 |
| NC_000014.7:g.22932750T>C | NCBI36 |
| NG_023444.1:g.19577A>G , LRG_389:g.19577A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000405093.9:c.2893A>G MANE Select | ENSP00000386041.3:p.Lys965Glu | |
| ENST00000356287.3:c.2893A>G | ENSP00000348634.3:p.Lys965Glu | |
| ENST00000405093.7:c.2893A>G | ENSP00000386041.3:p.Lys965Glu | |
| NM_002471.3:c.2893A>G , LRG_389t1:c.2893A>G | NP_002462.2:p.Lys965Glu | |
| NM_002471.4:c.2893A>G MANE Select | NP_002462.2:p.Lys965Glu |