Linked Data
MyVariant Identifiers:
chr14:g.50088730T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.49622012T>G , CM000676.2:g.49622012T>G | GRCh38 |
| NC_000014.8:g.50088730T>G , CM000676.1:g.50088730T>G | GRCh37 |
| NC_000014.7:g.49158480T>G | NCBI36 |
| NG_008920.1:g.6242T>G | |
| NG_033054.1:g.3620A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305386.4:c.744T>G MANE Select | ENSP00000307423.2:p.Leu248= | |
| ENST00000305386.3:c.744T>G | ENSP00000307423.2:p.Leu248= | |
| NM_002408.3:c.744T>G | NP_002399.1:p.Leu248= | |
| NM_002408.4:c.744T>G MANE Select | NP_002399.1:p.Leu248= |