Linked Data
MyVariant Identifiers:
chr21:g.43176817T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.41756657T>G , CM000683.2:g.41756657T>G | GRCh38 |
| NC_000021.8:g.43176817T>G , CM000683.1:g.43176817T>G | GRCh37 |
| NC_000021.7:g.42049886T>G | NCBI36 |
| NG_032113.1:g.15433A>C | |
| NG_032113.2:g.15433A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000332512.8:c.342A>C MANE Select | ENSP00000332454.3:p.Pro114= | |
| ENST00000332512.7:c.342A>C | ENSP00000332454.3:p.Pro114= | |
| ENST00000352483.3:c.342A>C | ENSP00000330161.2:p.Pro114= | |
| NM_020639.2:c.342A>C | NP_065690.2:p.Pro114= | |
| NM_020639.3:c.342A>C MANE Select | NP_065690.2:p.Pro114= |