Linked Data
MyVariant Identifiers:
chr5:g.14716882T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.14716773T>C , CM000667.2:g.14716773T>C | GRCh38 |
| NC_000005.9:g.14716882T>C , CM000667.1:g.14716882T>C | GRCh37 |
| NC_000005.8:g.14769882T>C | NCBI36 |
| NG_008273.1:g.160006A>G | |
| NG_008273.2:g.160013A>G | |
| NG_051625.1:g.60980T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000284268.8:c.1074A>G MANE Select | ENSP00000284268.6:p.Gly358= | |
| ENST00000284268.6:c.1074A>G | ENSP00000284268.6:p.Gly358= | |
| ENST00000502585.1:n.316A>G | ||
| NM_054027.4:c.1074A>G | NP_473368.1:p.Gly358= | |
| NM_054027.5:c.1074A>G | NP_473368.1:p.Gly358= | |
| XM_017009644.2:c.990A>G | XP_016865133.1:p.Gly330= | |
| NM_054027.6:c.1074A>G MANE Select | NP_473368.1:p.Gly358= |