Linked Data
ClinVar Variation Id:
365990
dbSNP Id:
rs371344592
ExAC:
9:140611142 G / A
gnomAD v2:
9-140611142-G-A
gnomAD v3:
9-137716690-G-A
gnomAD v4:
9-137716690-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.137716690G>A , CM000671.2:g.137716690G>A | GRCh38 |
| NC_000009.11:g.140611142G>A , CM000671.1:g.140611142G>A | GRCh37 |
| NC_000009.10:g.139730963G>A | NCBI36 |
| NG_011776.1:g.102699G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000460843.6:c.150G>A MANE Select | ENSP00000417980.1:p.Ala50= | |
| ENST00000629335.2:c.150G>A | ENSP00000490056.1:p.Ala50= | |
| ENST00000636027.1:c.57G>A | ENSP00000489961.1:p.Ala19= | |
| ENST00000637161.1:c.57G>A | ENSP00000490328.1:p.Ala19= | |
| ENST00000637261.1:c.126G>A | ENSP00000490815.1:p.Ala42= | |
| ENST00000637977.1:c.95G>A | ||
| ENST00000371394.6:c.86G>A | ENSP00000485945.1:p.Arg29Gln | |
| ENST00000460486.3:c.261G>A | ENSP00000486969.1:p.Ala87= | |
| ENST00000460843.5:c.150G>A | ENSP00000417980.1:p.Ala50= | |
| ENST00000462484.5:c.150G>A | ENSP00000417328.1:p.Ala50= | |
| ENST00000492232.5:c.57G>A | ENSP00000486580.1:p.Ala19= | |
| ENST00000626066.2:c.74G>A | ||
| ENST00000626216.2:c.57G>A | ENSP00000485878.1:p.Ala19= | |
| ENST00000629417.1:c.57G>A | ENSP00000486857.1:p.Ala19= | |
| ENST00000630754.2:c.57G>A | ENSP00000485933.1:p.Ala19= | |
| NM_001145527.1:c.150G>A | NP_001138999.1:p.Ala50= | |
| NM_024757.4:c.150G>A | NP_079033.4:p.Ala50= | |
| XM_005266105.3:c.141G>A | XP_005266162.1:p.Ala47= | |
| XM_005266110.1:c.57G>A | XP_005266167.1:p.Ala19= | |
| XM_006717288.2:c.132G>A | XP_006717351.1:p.Ala44= | |
| XM_011519021.1:c.159G>A | XP_011517323.1:p.Ala53= | |
| XM_011519022.1:c.156G>A | XP_011517324.1:p.Ala52= | |
| XM_011519023.1:c.159G>A | XP_011517325.1:p.Ala53= | |
| XM_011519024.1:c.159G>A | XP_011517326.1:p.Ala53= | |
| XM_011519025.1:c.57G>A | XP_011517327.1:p.Ala19= | |
| XM_011519026.1:c.159G>A | XP_011517328.1:p.Ala53= | |
| XM_011519027.1:c.159G>A | XP_011517329.1:p.Ala53= | |
| XM_011519028.1:c.159G>A | XP_011517330.1:p.Ala53= | |
| XM_011519033.1:c.159G>A | XP_011517335.1:p.Ala53= | |
| NM_001354259.1:c.57G>A | NP_001341188.1:p.Ala19= | |
| NM_001354263.1:c.150G>A | NP_001341192.1:p.Ala50= | |
| NM_001354611.1:c.150G>A | NP_001341540.1:p.Ala50= | |
| NM_001354612.1:c.57G>A | NP_001341541.1:p.Ala19= | |
| XM_005266105.5:c.141G>A | XP_005266162.1:p.Ala47= | |
| XM_011519021.3:c.159G>A | XP_011517323.1:p.Ala53= | |
| XM_011519022.3:c.156G>A | XP_011517324.1:p.Ala52= | |
| XM_011519023.3:c.159G>A | XP_011517325.1:p.Ala53= | |
| XM_017015134.1:c.156G>A | XP_016870623.1:p.Ala52= | |
| XM_017015136.2:c.150G>A | XP_016870625.1:p.Ala50= | |
| XM_017015137.1:c.57G>A | XP_016870626.1:p.Ala19= | |
| XM_017015138.1:c.57G>A | XP_016870627.1:p.Ala19= | |
| XM_024447674.1:c.57G>A | XP_024303442.1:p.Ala19= | |
| XM_024447675.1:c.57G>A | XP_024303443.1:p.Ala19= | |
| XM_024447678.1:c.57G>A | XP_024303446.1:p.Ala19= | |
| XM_024447679.1:c.57G>A | XP_024303447.1:p.Ala19= | |
| XM_024447680.1:c.57G>A | XP_024303448.1:p.Ala19= | |
| NM_024757.5:c.150G>A MANE Select | NP_079033.4:p.Ala50= | |
| NM_001145527.2:c.150G>A | NP_001138999.1:p.Ala50= | |
| NM_001354259.2:c.57G>A | NP_001341188.1:p.Ala19= | |
| NM_001354263.2:c.150G>A | NP_001341192.1:p.Ala50= | |
| NM_001354611.2:c.150G>A | NP_001341540.1:p.Ala50= | |
| NM_001354612.2:c.57G>A | NP_001341541.1:p.Ala19= |