Linked Data
dbSNP Id:
rs2096273751
gnomAD v3:
7-44146525-C-T
gnomAD v4:
7-44146525-C-T
MyVariant Identifiers:
chr7:g.44186124C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.44146525C>T , CM000669.2:g.44146525C>T | GRCh38 |
| NC_000007.13:g.44186124C>T , CM000669.1:g.44186124C>T | GRCh37 |
| NC_000007.12:g.44152649C>T | NCBI36 |
| NG_008847.1:g.47899G>A | |
| NG_008847.2:g.56646G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395796.8:c.*955G>A | ENSP00000379142.4:n.*955G>A | |
| ENST00000616242.5:c.*77G>A | ENSP00000482149.2:n.*77G>A | |
| ENST00000683378.1:n.183G>A | ||
| ENST00000345378.7:c.960G>A | ENSP00000223366.2:p.Glu320= | |
| ENST00000403799.8:c.957G>A MANE Select | ENSP00000384247.3:p.Glu319= | |
| ENST00000671824.1:c.1020G>A | ENSP00000500264.1:p.Glu340= | |
| ENST00000673284.1:c.957G>A | ENSP00000499852.1:p.Glu319= | |
| ENST00000345378.6:c.960G>A | ENSP00000223366.2:p.Glu320= | |
| ENST00000395796.7:c.954G>A | ENSP00000379142.3:p.Glu318= | |
| ENST00000403799.7:c.957G>A | ENSP00000384247.3:p.Glu319= | |
| ENST00000437084.1:c.906G>A | ENSP00000402840.1:p.Glu302= | |
| ENST00000473353.1:n.255G>A | ||
| ENST00000616242.4:c.954G>A | ENSP00000482149.1:p.Glu318= | |
| NM_000162.3:c.957G>A | NP_000153.1:p.Glu319= | |
| NM_033507.1:c.960G>A | NP_277042.1:p.Glu320= | |
| NM_033508.1:c.954G>A | NP_277043.1:p.Glu318= | |
| NM_000162.4:c.957G>A | NP_000153.1:p.Glu319= | |
| NM_001354800.1:c.957G>A | NP_001341729.1:p.Glu319= | |
| NM_001354801.1:c.8+94G>A | NP_001341730.1:n.8+94G>A | |
| NM_033507.2:c.960G>A | NP_277042.1:p.Glu320= | |
| NM_033508.2:c.954G>A | NP_277043.1:p.Glu318= | |
| NM_000162.5:c.957G>A MANE Select | NP_000153.1:p.Glu319= | |
| NM_033507.3:c.960G>A | NP_277042.1:p.Glu320= | |
| NM_033508.3:c.954G>A | NP_277043.1:p.Glu318= |