Linked Data
ClinVar Variation Id:
161259
dbSNP Id:
rs115585711
ExAC:
4:55564644 G / A
gnomAD v2:
4-55564644-G-A
gnomAD v3:
4-54698478-G-A
gnomAD v4:
4-54698478-G-A
PubMed:
PMID:25637381
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.54698478G>A , CM000666.2:g.54698478G>A | GRCh38 |
| NC_000004.11:g.55564644G>A , CM000666.1:g.55564644G>A | GRCh37 |
| NC_000004.10:g.55259401G>A | NCBI36 |
| NG_007456.1:g.45484G>A , LRG_307:g.45484G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000412167.7:c.532G>A | ENSP00000390987.3:p.Ala178Thr | |
| ENST00000685269.1:n.610G>A | ||
| ENST00000686011.1:c.532G>A | ENSP00000509704.1:p.Ala178Thr | |
| ENST00000687109.1:c.532G>A | ENSP00000509371.1:p.Ala178Thr | |
| ENST00000687208.1:n.947G>A | ||
| ENST00000687246.1:c.532G>A | ENSP00000509114.1:p.Ala178Thr | |
| ENST00000687265.1:n.702G>A | ||
| ENST00000687295.1:c.532G>A | ENSP00000509450.1:p.Ala178Thr | |
| ENST00000689832.1:c.532G>A | ENSP00000509084.1:p.Ala178Thr | |
| ENST00000689994.1:c.22G>A | ENSP00000509156.1:p.Ala8Thr | |
| ENST00000690519.1:c.532G>A | ENSP00000508845.1:p.Ala178Thr | |
| ENST00000690543.1:c.532G>A | ENSP00000508831.1:p.Ala178Thr | |
| ENST00000690917.1:n.750G>A | ||
| ENST00000692783.1:c.532G>A | ENSP00000508733.1:p.Ala178Thr | |
| ENST00000692991.1:n.641G>A | ||
| ENST00000288135.6:c.532G>A MANE Select | ENSP00000288135.6:p.Ala178Thr | |
| ENST00000288135.5:c.532G>A | ENSP00000288135.5:p.Ala178Thr | |
| ENST00000412167.6:c.532G>A | ENSP00000390987.2:p.Ala178Thr | |
| NM_000222.2:c.532G>A , LRG_307t1:c.532G>A | NP_000213.1:p.Ala178Thr | |
| NM_001093772.1:c.532G>A | NP_001087241.1:p.Ala178Thr | |
| XM_005265740.1:c.532G>A | XP_005265797.1:p.Ala178Thr | |
| XM_005265741.1:c.532G>A | XP_005265798.1:p.Ala178Thr | |
| XM_005265742.1:c.532G>A | XP_005265799.1:p.Ala178Thr | |
| XM_005265742.3:c.532G>A | XP_005265799.1:p.Ala178Thr | |
| XM_017008178.1:c.532G>A | XP_016863667.1:p.Ala178Thr | |
| XM_017008179.1:c.532G>A | XP_016863668.1:p.Ala178Thr | |
| XM_017008180.1:c.532G>A | XP_016863669.1:p.Ala178Thr | |
| NM_000222.3:c.532G>A MANE Select | NP_000213.1:p.Ala178Thr | |
| NM_001093772.2:c.532G>A | NP_001087241.1:p.Ala178Thr | |
| NM_001385284.1:c.532G>A | NP_001372213.1:p.Ala178Thr | |
| NM_001385285.1:c.532G>A | NP_001372214.1:p.Ala178Thr | |
| NM_001385286.1:c.532G>A | NP_001372215.1:p.Ala178Thr | |
| NM_001385288.1:c.532G>A | NP_001372217.1:p.Ala178Thr | |
| NM_001385290.1:c.532G>A | NP_001372219.1:p.Ala178Thr | |
| NM_001385292.1:c.532G>A | NP_001372221.1:p.Ala178Thr |