MyVariant.info:
GRCh38
chr21:g.43417679G>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.43417679G>A , CM000683.2:g.43417679G>A | GRCh38 |
| NG_052009.1:g.14454C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270162.8:c.1840C>T MANE Select | ENSP00000270162.6:p.Gln614Ter | |
| ENST00000270162.6:c.1840C>T | ENSP00000270162.6:p.Gln614Ter | |
| NM_173354.3:c.1840C>T | NP_775490.2:p.Gln614Ter | |
| XM_011529474.1:c.1693C>T | XP_011527776.1:p.Gln565Ter | |
| NM_173354.4:c.1840C>T | NP_775490.2:p.Gln614Ter | |
| XM_011529474.2:c.1693C>T | XP_011527776.1:p.Gln565Ter | |
| NM_173354.5:c.1840C>T MANE Select | NP_775490.2:p.Gln614Ter |