Linked Data
dbSNP Id:
rs1787720981
gnomAD v3:
7-5641337-G-A
gnomAD v4:
7-5641337-G-A
MyVariant Identifiers:
chr7:g.5680968G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.5641337G>A , CM000669.2:g.5641337G>A | GRCh38 |
| NC_000007.13:g.5680968G>A , CM000669.1:g.5680968G>A | GRCh37 |
| NC_000007.12:g.5647494G>A | NCBI36 |
| NG_029374.1:g.145394C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389902.8:c.2199C>T MANE Select | ENSP00000374552.3:p.His733= | |
| ENST00000389900.8:c.*1316C>T | ENSP00000374550.4:n.*1316C>T | |
| ENST00000389902.7:c.2199C>T | ENSP00000374552.3:p.His733= | |
| ENST00000425013.6:c.2028C>T | ENSP00000404602.2:p.His676= | |
| ENST00000469375.1:n.416C>T | ||
| NM_207111.3:c.2199C>T | NP_996994.1:p.His733= | |
| NM_207116.2:c.2028C>T | NP_996999.1:p.His676= | |
| XM_005249785.2:c.2199C>T | XP_005249842.1:p.His733= | |
| XM_006715748.1:c.894C>T | XP_006715811.1:p.His298= | |
| XM_011515434.1:c.2199C>T | XP_011513736.1:p.His733= | |
| XM_011515436.1:c.894C>T | XP_011513738.1:p.His298= | |
| XM_011515436.2:c.894C>T | XP_011513738.1:p.His298= | |
| XM_017012363.2:c.2028C>T | XP_016867852.1:p.His676= | |
| XM_024446805.1:c.2199C>T | XP_024302573.1:p.His733= | |
| XM_024446806.1:c.894C>T | XP_024302574.1:p.His298= | |
| XM_024446807.1:c.894C>T | XP_024302575.1:p.His298= | |
| NM_001377156.1:c.2028C>T | NP_001364085.1:p.His676= | |
| NM_207111.4:c.2199C>T MANE Select | NP_996994.1:p.His733= | |
| NM_207116.3:c.2028C>T | NP_996999.1:p.His676= |