Linked Data
dbSNP Id:
rs1487669494
gnomAD v2:
5-7878009-G-A
gnomAD v3:
5-7877896-G-A
gnomAD v4:
5-7877896-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.7877896G>A , CM000667.2:g.7877896G>A | GRCh38 |
| NC_000005.9:g.7878009G>A , CM000667.1:g.7878009G>A | GRCh37 |
| NC_000005.8:g.7931009G>A | NCBI36 |
| NG_008856.1:g.13793G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000440940.7:c.402-48G>A MANE Select | ENSP00000402510.2:n.402-48G>A | |
| ENST00000264668.6:c.483-48G>A | ENSP00000264668.2:n.483-48G>A | |
| ENST00000440940.6:c.402-48G>A | ENSP00000402510.2:n.402-48G>A | |
| ENST00000502509.5:n.617-48G>A | ||
| ENST00000502550.5:c.402-48G>A | ENSP00000424599.1:n.402-48G>A | |
| ENST00000503550.5:c.*337-48G>A | ENSP00000424644.1:n.*337-48G>A | |
| ENST00000508047.5:c.455-48G>A | ||
| ENST00000508890.1:n.215-48G>A | ||
| ENST00000510279.5:c.*71-48G>A | ENSP00000427200.1:n.*71-48G>A | |
| ENST00000510525.5:c.427-48G>A | ||
| ENST00000511461.5:c.315-48G>A | ||
| ENST00000513439.5:c.*109-48G>A | ENSP00000426710.1:n.*109-48G>A | |
| ENST00000514220.5:c.187-48G>A | ||
| ENST00000514369.5:c.*71-53G>A | ENSP00000426132.1:n.*71-53G>A | |
| NM_002454.2:c.402-48G>A | NP_002445.2:n.402-48G>A | |
| NM_024010.2:c.483-48G>A | NP_076915.2:n.483-48G>A | |
| XM_006714474.2:c.483-48G>A | XP_006714537.1:n.483-48G>A | |
| XM_011514043.1:c.483-48G>A | XP_011512345.1:n.483-48G>A | |
| XM_011514044.1:c.402-48G>A | XP_011512346.1:n.402-48G>A | |
| XM_011514045.1:c.483-48G>A | XP_011512347.1:n.483-48G>A | |
| XR_241702.1:n.505-48G>A | ||
| XR_241703.1:n.498-48G>A | ||
| XR_925614.1:n.505-48G>A | ||
| XR_925615.1:n.505-48G>A | ||
| NM_001364440.1:c.402-48G>A | NP_001351369.1:n.402-48G>A | |
| NM_001364441.1:c.402-48G>A | NP_001351370.1:n.402-48G>A | |
| NM_001364442.1:c.402-48G>A | NP_001351371.1:n.402-48G>A | |
| NM_024010.3:c.402-48G>A | NP_076915.3:n.402-48G>A | |
| NR_134480.1:n.525-48G>A | ||
| NR_134481.1:n.539-48G>A | ||
| NR_134482.1:n.385-48G>A | ||
| NR_157168.1:n.455-48G>A | ||
| NR_157169.1:n.315-48G>A | ||
| NR_157170.1:n.341-48G>A | ||
| NR_157171.1:n.315-48G>A | ||
| NR_157172.1:n.341-48G>A | ||
| NR_157173.1:n.469-48G>A | ||
| NR_157174.1:n.341-48G>A | ||
| NR_157175.1:n.495-48G>A | ||
| NR_157176.1:n.495-48G>A | ||
| NR_157177.1:n.495-53G>A | ||
| NR_157178.1:n.495-48G>A | ||
| XM_024446063.1:c.447-48G>A | XP_024301831.1:n.447-48G>A | |
| XM_024446064.1:c.402-48G>A | XP_024301832.1:n.402-48G>A | |
| XR_001742071.1:n.505-48G>A | ||
| XR_001742072.1:n.505-48G>A | ||
| XR_001742074.1:n.505-48G>A | ||
| XR_001742075.1:n.505-48G>A | ||
| XR_001742076.1:n.505-48G>A | ||
| XR_001742077.1:n.505-48G>A | ||
| NM_001364440.2:c.402-48G>A | NP_001351369.1:n.402-48G>A | |
| NM_001364441.2:c.402-48G>A | NP_001351370.1:n.402-48G>A | |
| NM_001364442.2:c.402-48G>A | NP_001351371.1:n.402-48G>A | |
| NM_002454.3:c.402-48G>A MANE Select | NP_002445.2:n.402-48G>A | |
| NM_024010.4:c.402-48G>A | NP_076915.3:n.402-48G>A | |
| NR_134480.2:n.481-48G>A | ||
| NR_134481.2:n.495-48G>A | ||
| NR_134482.2:n.341-48G>A | ||
| NR_157168.2:n.455-48G>A | ||
| NR_157169.2:n.315-48G>A | ||
| NR_157170.2:n.341-48G>A | ||
| NR_157171.2:n.315-48G>A | ||
| NR_157172.2:n.341-48G>A | ||
| NR_157173.2:n.469-48G>A | ||
| NR_157174.2:n.341-48G>A | ||
| NR_157175.2:n.495-48G>A | ||
| NR_157176.2:n.495-48G>A | ||
| NR_157177.2:n.495-53G>A | ||
| NR_157178.2:n.495-48G>A |