Linked Data
dbSNP Id:
rs773160237
ExAC:
5:7878184 A / G
gnomAD v2:
5-7878184-A-G
gnomAD v4:
5-7878071-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.7878071A>G , CM000667.2:g.7878071A>G | GRCh38 |
| NC_000005.9:g.7878184A>G , CM000667.1:g.7878184A>G | GRCh37 |
| NC_000005.8:g.7931184A>G | NCBI36 |
| NG_008856.1:g.13968A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000440940.7:c.529A>G MANE Select | ENSP00000402510.2:p.Thr177Ala | |
| ENST00000264668.6:c.610A>G | ENSP00000264668.2:p.Thr204Ala | |
| ENST00000440940.6:c.529A>G | ENSP00000402510.2:p.Thr177Ala | |
| ENST00000508890.1:n.342A>G | ||
| ENST00000510279.5:c.*198A>G | ENSP00000427200.1:n.*198A>G | |
| ENST00000510525.5:c.554A>G | ||
| ENST00000511461.5:c.442A>G | ||
| ENST00000513439.5:c.*236A>G | ENSP00000426710.1:n.*236A>G | |
| ENST00000514220.5:c.314A>G | ||
| ENST00000514369.5:c.*193A>G | ENSP00000426132.1:n.*193A>G | |
| NM_002454.2:c.529A>G | NP_002445.2:p.Thr177Ala | |
| NM_024010.2:c.610A>G | NP_076915.2:p.Thr204Ala | |
| XM_006714474.2:c.610A>G | XP_006714537.1:p.Thr204Ala | |
| XM_011514043.1:c.610A>G | XP_011512345.1:p.Thr204Ala | |
| XM_011514044.1:c.529A>G | XP_011512346.1:p.Thr177Ala | |
| XM_011514045.1:c.610A>G | XP_011512347.1:p.Thr204Ala | |
| XR_241702.1:n.632A>G | ||
| XR_241703.1:n.625A>G | ||
| XR_925614.1:n.632A>G | ||
| XR_925615.1:n.632A>G | ||
| NM_001364440.1:c.529A>G | NP_001351369.1:p.Thr177Ala | |
| NM_001364441.1:c.529A>G | NP_001351370.1:p.Thr177Ala | |
| NM_001364442.1:c.529A>G | NP_001351371.1:p.Thr177Ala | |
| NM_024010.3:c.529A>G | NP_076915.3:p.Thr177Ala | |
| NR_134480.1:n.652A>G | ||
| NR_134481.1:n.666A>G | ||
| NR_134482.1:n.512A>G | ||
| NR_157168.1:n.582A>G | ||
| NR_157169.1:n.442A>G | ||
| NR_157170.1:n.468A>G | ||
| NR_157171.1:n.442A>G | ||
| NR_157172.1:n.468A>G | ||
| NR_157173.1:n.596A>G | ||
| NR_157174.1:n.468A>G | ||
| NR_157175.1:n.622A>G | ||
| NR_157176.1:n.622A>G | ||
| NR_157177.1:n.617A>G | ||
| NR_157178.1:n.622A>G | ||
| XM_024446063.1:c.574A>G | XP_024301831.1:p.Thr192Ala | |
| XM_024446064.1:c.529A>G | XP_024301832.1:p.Thr177Ala | |
| XR_001742071.1:n.632A>G | ||
| XR_001742072.1:n.632A>G | ||
| XR_001742074.1:n.632A>G | ||
| XR_001742075.1:n.632A>G | ||
| XR_001742076.1:n.632A>G | ||
| XR_001742077.1:n.632A>G | ||
| NM_001364440.2:c.529A>G | NP_001351369.1:p.Thr177Ala | |
| NM_001364441.2:c.529A>G | NP_001351370.1:p.Thr177Ala | |
| NM_001364442.2:c.529A>G | NP_001351371.1:p.Thr177Ala | |
| NM_002454.3:c.529A>G MANE Select | NP_002445.2:p.Thr177Ala | |
| NM_024010.4:c.529A>G | NP_076915.3:p.Thr177Ala | |
| NR_134480.2:n.608A>G | ||
| NR_134481.2:n.622A>G | ||
| NR_134482.2:n.468A>G | ||
| NR_157168.2:n.582A>G | ||
| NR_157169.2:n.442A>G | ||
| NR_157170.2:n.468A>G | ||
| NR_157171.2:n.442A>G | ||
| NR_157172.2:n.468A>G | ||
| NR_157173.2:n.596A>G | ||
| NR_157174.2:n.468A>G | ||
| NR_157175.2:n.622A>G | ||
| NR_157176.2:n.622A>G | ||
| NR_157177.2:n.617A>G | ||
| NR_157178.2:n.622A>G |