Linked Data
ClinVar Variation Id:
203601
dbSNP Id:
rs144681140
ExAC:
16:89211714 G / A
gnomAD v2:
16-89211714-G-A
gnomAD v3:
16-89145306-G-A
gnomAD v4:
16-89145306-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89145306G>A , CM000678.2:g.89145306G>A | GRCh38 |
| NC_000016.9:g.89211714G>A , CM000678.1:g.89211714G>A | GRCh37 |
| NC_000016.8:g.87739215G>A | NCBI36 |
| NG_031961.1:g.56498G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000317447.9:c.1406G>A | ENSP00000320646.4:p.Arg469Gln | |
| ENST00000614302.5:c.1406G>A MANE Select | ENSP00000479130.1:p.Arg469Gln | |
| ENST00000649953.1:c.1616G>A | ENSP00000497456.1:p.Arg539Gln | |
| ENST00000317447.8:c.1406G>A | ENSP00000320646.4:p.Arg469Gln | |
| ENST00000378345.8:c.611G>A | ENSP00000367596.4:p.Arg204Gln | |
| ENST00000406948.7:c.1406G>A | ENSP00000384627.3:p.Arg469Gln | |
| ENST00000537116.5:n.532G>A | ||
| ENST00000537155.1:n.146G>A | ||
| ENST00000542688.5:c.*150G>A | ENSP00000446281.1:n.*150G>A | |
| ENST00000544543.5:c.611G>A | ENSP00000442781.1:p.Arg204Gln | |
| ENST00000562204.1:n.379G>A | ||
| ENST00000614302.4:c.1406G>A | ENSP00000479130.1:p.Arg469Gln | |
| NM_001127214.3:c.1406G>A | NP_001120686.1:p.Arg469Gln | |
| NM_001243279.2:c.1406G>A | NP_001230208.1:p.Arg469Gln | |
| NM_001284316.1:c.611G>A | NP_001271245.1:p.Arg204Gln | |
| NM_174917.4:c.1406G>A | NP_777577.2:p.Arg469Gln | |
| NR_045667.2:n.532G>A | ||
| NR_104293.1:n.1840G>A | ||
| XM_005256293.1:c.1406G>A | XP_005256350.1:p.Arg469Gln | |
| XM_011522942.1:c.1406G>A | XP_011521244.1:p.Arg469Gln | |
| XM_011522943.1:c.1406G>A | XP_011521245.1:p.Arg469Gln | |
| XR_933239.1:n.1847G>A | ||
| XR_933240.1:n.1844G>A | ||
| XR_933241.1:n.1601G>A | ||
| NR_147928.1:n.1884G>A | ||
| NR_147929.1:n.1638G>A | ||
| XM_005256293.2:c.1406G>A | XP_005256350.1:p.Arg469Gln | |
| XM_017023018.1:c.1406G>A | XP_016878507.1:p.Arg469Gln | |
| XM_017023019.1:c.1406G>A | XP_016878508.1:p.Arg469Gln | |
| XM_017023020.2:c.-3699G>A | XP_016878509.1:n.-3699G>A | |
| XM_017023022.1:c.539G>A | XP_016878511.1:p.Arg180Gln | |
| XM_024450186.1:c.611G>A | XP_024305954.1:p.Arg204Gln | |
| XM_024450187.1:c.611G>A | XP_024305955.1:p.Arg204Gln | |
| XR_001751864.2:n.1653G>A | ||
| XR_001751865.1:n.1600G>A | ||
| XR_933240.3:n.1843G>A | ||
| NM_001127214.4:c.1406G>A | NP_001120686.1:p.Arg469Gln | |
| NM_001243279.3:c.1406G>A MANE Select | NP_001230208.1:p.Arg469Gln | |
| NM_001284316.2:c.611G>A | NP_001271245.1:p.Arg204Gln | |
| NM_174917.5:c.1406G>A | NP_777577.2:p.Arg469Gln | |
| NR_104293.2:n.1797G>A | ||
| NR_147928.2:n.1841G>A | ||
| NR_147929.2:n.1595G>A |