Linked Data
MyVariant Identifiers:
chr5:g.14716912C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.14716803C>T , CM000667.2:g.14716803C>T | GRCh38 |
| NC_000005.9:g.14716912C>T , CM000667.1:g.14716912C>T | GRCh37 |
| NC_000005.8:g.14769912C>T | NCBI36 |
| NG_008273.1:g.159976G>A | |
| NG_008273.2:g.159983G>A | |
| NG_051625.1:g.61010C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000284268.8:c.1044G>A MANE Select | ENSP00000284268.6:p.Val348= | |
| ENST00000284268.6:c.1044G>A | ENSP00000284268.6:p.Val348= | |
| ENST00000502585.1:n.286G>A | ||
| NM_054027.4:c.1044G>A | NP_473368.1:p.Val348= | |
| NM_054027.5:c.1044G>A | NP_473368.1:p.Val348= | |
| XM_017009644.2:c.960G>A | XP_016865133.1:p.Val320= | |
| NM_054027.6:c.1044G>A MANE Select | NP_473368.1:p.Val348= |