Linked Data
dbSNP Id:
rs1444146990
gnomAD v4:
9-2116031-G-A
MyVariant Identifiers:
chr9:g.2116031G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.2116031G>A , CM000671.2:g.2116031G>A | GRCh38 |
| NC_000009.11:g.2116031G>A , CM000671.1:g.2116031G>A | GRCh37 |
| NC_000009.10:g.2106031G>A | NCBI36 |
| NG_032162.1:g.105690G>A | |
| NG_032162.2:g.140742G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000704350.1:c.3306G>A | ENSP00000515861.1:p.Glu1102= | |
| ENST00000704352.1:c.1174-45655G>A | ENSP00000515863.1:n.1174-45655G>A | |
| ENST00000704353.1:c.1174-45655G>A | ENSP00000515864.1:n.1174-45655G>A | |
| ENST00000704354.1:c.3650G>A | ||
| ENST00000704355.1:c.2030G>A | ||
| ENST00000349721.8:c.3666G>A MANE Select | ENSP00000265773.5:p.Glu1222= | |
| ENST00000357248.8:c.3666G>A | ENSP00000349788.2:p.Glu1222= | |
| ENST00000635739.1:n.2334G>A | ||
| ENST00000636157.1:n.1273G>A | ||
| ENST00000638139.1:n.700G>A | ||
| ENST00000349721.7:c.3666G>A | ENSP00000265773.5:p.Glu1222= | |
| ENST00000357248.7:c.3666G>A | ENSP00000349788.2:p.Glu1222= | |
| ENST00000382194.6:c.3666G>A | ENSP00000371629.1:p.Glu1222= | |
| ENST00000382203.5:c.3666G>A | ENSP00000371638.1:p.Glu1222= | |
| ENST00000450198.6:c.3492G>A | ENSP00000392081.2:p.Glu1164= | |
| ENST00000634760.1:c.3666G>A | ENSP00000489256.1:p.Glu1222= | |
| ENST00000634772.1:c.62-3427G>A | ||
| ENST00000634925.1:n.1157G>A | ||
| NM_001289396.1:c.3666G>A | NP_001276325.1:p.Glu1222= | |
| NM_001289397.1:c.3492G>A | NP_001276326.1:p.Glu1164= | |
| NM_003070.4:c.3666G>A | NP_003061.3:p.Glu1222= | |
| NM_139045.3:c.3666G>A | NP_620614.2:p.Glu1222= | |
| NM_003070.5:c.3666G>A MANE Select | NP_003061.3:p.Glu1222= | |
| NM_001289397.2:c.3492G>A | NP_001276326.1:p.Glu1164= | |
| NM_139045.4:c.3666G>A | NP_620614.2:p.Glu1222= |