Linked Data
MyVariant Identifiers:
chr14:g.50088601T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.49621883T>G , CM000676.2:g.49621883T>G | GRCh38 |
| NC_000014.8:g.50088601T>G , CM000676.1:g.50088601T>G | GRCh37 |
| NC_000014.7:g.49158351T>G | NCBI36 |
| NG_008920.1:g.6113T>G | |
| NG_033054.1:g.3749A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000305386.4:c.615T>G MANE Select | ENSP00000307423.2:p.Ala205= | |
| ENST00000305386.3:c.615T>G | ENSP00000307423.2:p.Ala205= | |
| NM_002408.3:c.615T>G | NP_002399.1:p.Ala205= | |
| NM_002408.4:c.615T>G MANE Select | NP_002399.1:p.Ala205= |