Linked Data
dbSNP Id:
rs760386808
gnomAD v3:
21-44886871-G-T
gnomAD v4:
21-44886871-G-T
MyVariant Identifiers:
chr21:g.46306786G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44886871G>T , CM000683.2:g.44886871G>T | GRCh38 |
| NC_000021.8:g.46306786G>T , CM000683.1:g.46306786G>T | GRCh37 |
| NC_000021.7:g.45131214G>T | NCBI36 |
| NG_007270.2:g.46968C>A , LRG_76:g.46968C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696946.1:n.1319C>A | ||
| ENST00000302347.10:c.2184C>A | ENSP00000303242.6:p.Ile728= | |
| ENST00000652462.1:c.2112C>A MANE Select | ENSP00000498780.1:p.Ile704= | |
| ENST00000302347.9:c.2112C>A | ENSP00000303242.5:p.Ile704= | |
| ENST00000355153.8:c.2112C>A | ENSP00000347279.4:p.Ile704= | |
| ENST00000397850.6:c.2112C>A | ENSP00000380948.2:p.Ile704= | |
| ENST00000397852.5:c.2112C>A | ENSP00000380950.1:p.Ile704= | |
| ENST00000397854.7:c.1941C>A | ENSP00000380952.3:p.Ile647= | |
| ENST00000397857.5:c.2112C>A | ENSP00000380955.1:p.Ile704= | |
| ENST00000475170.5:n.1512C>A | ||
| ENST00000479202.5:n.471C>A | ||
| ENST00000498666.5:n.4168C>A | ||
| ENST00000523323.5:c.*1939C>A | ENSP00000427732.1:n.*1939C>A | |
| ENST00000610622.4:c.*803C>A | ENSP00000480700.1:n.*803C>A | |
| NM_000211.4:c.2112C>A | NP_000202.3:p.Ile704= | |
| NM_001127491.2:c.2112C>A | NP_001120963.2:p.Ile704= | |
| NM_001303238.1:c.1905C>A | NP_001290167.1:p.Ile635= | |
| XM_006724001.1:c.1905C>A | XP_006724064.1:p.Ile635= | |
| XM_006724001.2:c.1905C>A | XP_006724064.1:p.Ile635= | |
| NM_000211.5:c.2112C>A MANE Select | NP_000202.3:p.Ile704= | |
| NM_001127491.3:c.2112C>A | NP_001120963.2:p.Ile704= | |
| NM_001303238.2:c.1905C>A | NP_001290167.1:p.Ile635= |