Linked Data
ClinVar Variation Id:
7119
ClinVar RCV Id:
RCV000007539
RCV001009367
RCV001004269
RCV001831523
RCV002254259
RCV002490333
RCV003473008
dbSNP Id:
rs121908758
gnomAD v2:
7-117230448-C-A
gnomAD v3:
7-117590394-C-A
gnomAD v4:
7-117590394-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117590394C>A , CM000669.2:g.117590394C>A | GRCh38 |
| NC_000007.13:g.117230448C>A , CM000669.1:g.117230448C>A | GRCh37 |
| NC_000007.12:g.117017684C>A | NCBI36 |
| NG_016465.4:g.129611C>A , LRG_663:g.129611C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647720.2:c.1721C>A | ENSP00000497673.2:p.Pro574His | |
| ENST00000647978.2:c.*1435C>A | ENSP00000497658.1:n.*1435C>A | |
| ENST00000649781.2:c.1538C>A | ENSP00000497203.1:p.Pro513His | |
| ENST00000685018.2:c.1721C>A | ENSP00000510194.2:p.Pro574His | |
| ENST00000687278.2:c.1721C>A | ENSP00000509593.2:p.Pro574His | |
| ENST00000699585.1:c.1721C>A | ENSP00000514456.1:p.Pro574His | |
| ENST00000699598.1:c.1721C>A | ENSP00000514467.1:p.Pro574His | |
| ENST00000699599.1:c.1721C>A | ENSP00000514468.1:p.Pro574His | |
| ENST00000699600.1:c.1721C>A | ENSP00000514469.1:p.Pro574His | |
| ENST00000699601.1:c.*21C>A | ENSP00000514470.1:n.*21C>A | |
| ENST00000699602.1:c.1721C>A | ENSP00000514471.1:p.Pro574His | |
| ENST00000699604.1:c.*1545C>A | ENSP00000514472.1:n.*1545C>A | |
| ENST00000699605.1:c.1295C>A | ENSP00000514473.1:p.Pro432His | |
| ENST00000003084.11:c.1721C>A MANE Select | ENSP00000003084.6:p.Pro574His | |
| ENST00000647978.1:c.*1435C>A | ENSP00000497658.1:n.*1435C>A | |
| ENST00000648260.1:c.1402-12432C>A | ENSP00000497957.1:n.1402-12432C>A | |
| ENST00000649406.1:c.1538C>A | ENSP00000497965.1:p.Pro513His | |
| ENST00000649781.1:c.1538C>A | ENSP00000497203.1:p.Pro513His | |
| ENST00000003084.10:c.1721C>A | ENSP00000003084.6:p.Pro574His | |
| ENST00000426809.5:c.1631C>A | ENSP00000389119.1:p.Pro544His | |
| NM_000492.3:c.1721C>A , LRG_663t1:c.1721C>A | NP_000483.3:p.Pro574His | |
| XM_011515751.1:c.1811C>A | XP_011514053.1:p.Pro604His | |
| XM_011515752.1:c.1811C>A | XP_011514054.1:p.Pro604His | |
| XM_011515753.1:c.1478C>A | XP_011514055.1:p.Pro493His | |
| XM_011515754.1:c.1478C>A | XP_011514056.1:p.Pro493His | |
| NM_000492.4:c.1721C>A MANE Select | NP_000483.3:p.Pro574His |