MyVariant.info:
GRCh37
chr21:g.46311813A>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44891898A>T , CM000683.2:g.44891898A>T | GRCh38 |
| NC_000021.8:g.46311813A>T , CM000683.1:g.46311813A>T | GRCh37 |
| NC_000021.7:g.45136241A>T | NCBI36 |
| NG_007270.2:g.41941T>A , LRG_76:g.41941T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696946.1:n.530T>A | ||
| ENST00000302347.10:c.1395T>A | ENSP00000303242.6:p.Val465= | |
| ENST00000652462.1:c.1323T>A MANE Select | ENSP00000498780.1:p.Val441= | |
| ENST00000302347.9:c.1323T>A | ENSP00000303242.5:p.Val441= | |
| ENST00000355153.8:c.1323T>A | ENSP00000347279.4:p.Val441= | |
| ENST00000397850.6:c.1323T>A | ENSP00000380948.2:p.Val441= | |
| ENST00000397852.5:c.1323T>A | ENSP00000380950.1:p.Val441= | |
| ENST00000397854.7:c.1152T>A | ENSP00000380952.3:p.Val384= | |
| ENST00000397857.5:c.1323T>A | ENSP00000380955.1:p.Val441= | |
| ENST00000475170.5:n.723T>A | ||
| ENST00000498666.5:n.3379T>A | ||
| ENST00000523323.5:c.*1150T>A | ENSP00000427732.1:n.*1150T>A | |
| ENST00000610622.4:c.*14T>A | ENSP00000480700.1:n.*14T>A | |
| NM_000211.4:c.1323T>A | NP_000202.3:p.Val441= | |
| NM_001127491.2:c.1323T>A | NP_001120963.2:p.Val441= | |
| NM_001303238.1:c.1116T>A | NP_001290167.1:p.Val372= | |
| XM_006724001.1:c.1116T>A | XP_006724064.1:p.Val372= | |
| XM_006724001.2:c.1116T>A | XP_006724064.1:p.Val372= | |
| NM_000211.5:c.1323T>A MANE Select | NP_000202.3:p.Val441= | |
| NM_001127491.3:c.1323T>A | NP_001120963.2:p.Val441= | |
| NM_001303238.2:c.1116T>A | NP_001290167.1:p.Val372= |