Linked Data
MyVariant Identifiers:
chr5:g.14716921T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.14716812T>C , CM000667.2:g.14716812T>C | GRCh38 |
| NC_000005.9:g.14716921T>C , CM000667.1:g.14716921T>C | GRCh37 |
| NC_000005.8:g.14769921T>C | NCBI36 |
| NG_008273.1:g.159967A>G | |
| NG_008273.2:g.159974A>G | |
| NG_051625.1:g.61019T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000284268.8:c.1035A>G MANE Select | ENSP00000284268.6:p.Thr345= | |
| ENST00000284268.6:c.1035A>G | ENSP00000284268.6:p.Thr345= | |
| ENST00000502585.1:n.277A>G | ||
| NM_054027.4:c.1035A>G | NP_473368.1:p.Thr345= | |
| NM_054027.5:c.1035A>G | NP_473368.1:p.Thr345= | |
| XM_017009644.2:c.951A>G | XP_016865133.1:p.Thr317= | |
| NM_054027.6:c.1035A>G MANE Select | NP_473368.1:p.Thr345= |