Linked Data
gnomAD v4:
14-49622058-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.49622058T>G , CM000676.2:g.49622058T>G | GRCh38 |
| NC_000014.8:g.50088776T>G , CM000676.1:g.50088776T>G | GRCh37 |
| NC_000014.7:g.49158526T>G | NCBI36 |
| NG_008920.1:g.6288T>G | |
| NG_033054.1:g.3574A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000305386.4:c.790T>G MANE Select | ENSP00000307423.2:p.Leu264Val | |
| ENST00000305386.3:c.790T>G | ENSP00000307423.2:p.Leu264Val | |
| NM_002408.3:c.790T>G | NP_002399.1:p.Leu264Val | |
| NM_002408.4:c.790T>G MANE Select | NP_002399.1:p.Leu264Val |