Linked Data
MyVariant Identifiers:
chr21:g.45681053T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44261170T>A , CM000683.2:g.44261170T>A | GRCh38 |
| NC_000021.8:g.45681053T>A , CM000683.1:g.45681053T>A | GRCh37 |
| NC_000021.7:g.44505481T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000628202.3:c.90A>T MANE Select | ENSP00000486001.1:p.Ser30= | |
| ENST00000270172.7:c.90A>T | ENSP00000270172.3:p.Ser30= | |
| ENST00000431166.1:c.90A>T | ENSP00000400242.1:p.Ser30= | |
| ENST00000628202.2:c.90A>T | ENSP00000486001.1:p.Ser30= | |
| NM_013369.3:c.90A>T | NP_037501.2:p.Ser30= | |
| NM_175867.2:c.90A>T | NP_787063.1:p.Ser30= | |
| XM_011529536.1:c.90A>T | XP_011527838.1:p.Ser30= | |
| NM_013369.4:c.90A>T | NP_037501.2:p.Ser30= | |
| NM_175867.3:c.90A>T MANE Select | NP_787063.1:p.Ser30= |