Linked Data
MyVariant Identifiers:
chr5:g.14716864T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.14716755T>A , CM000667.2:g.14716755T>A | GRCh38 |
| NC_000005.9:g.14716864T>A , CM000667.1:g.14716864T>A | GRCh37 |
| NC_000005.8:g.14769864T>A | NCBI36 |
| NG_008273.1:g.160024A>T | |
| NG_008273.2:g.160031A>T | |
| NG_051625.1:g.60962T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000284268.8:c.1092A>T MANE Select | ENSP00000284268.6:p.Ala364= | |
| ENST00000284268.6:c.1092A>T | ENSP00000284268.6:p.Ala364= | |
| ENST00000502585.1:n.334A>T | ||
| NM_054027.4:c.1092A>T | NP_473368.1:p.Ala364= | |
| NM_054027.5:c.1092A>T | NP_473368.1:p.Ala364= | |
| XM_017009644.2:c.1008A>T | XP_016865133.1:p.Ala336= | |
| NM_054027.6:c.1092A>T MANE Select | NP_473368.1:p.Ala364= |