Linked Data
MyVariant Identifiers:
chr21:g.45876614G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44456731G>C , CM000683.2:g.44456731G>C | GRCh38 |
| NC_000021.8:g.45876614G>C , CM000683.1:g.45876614G>C | GRCh37 |
| NC_000021.7:g.44701042G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291592.6:c.87G>C MANE Select | ENSP00000291592.4:p.Leu29= | |
| ENST00000291592.5:c.87G>C | ENSP00000291592.4:p.Leu29= | |
| NM_030891.4:c.87G>C | NP_112153.1:p.Leu29= | |
| NM_030891.5:c.87G>C | NP_112153.1:p.Leu29= | |
| NM_030891.6:c.87G>C MANE Select | NP_112153.1:p.Leu29= |