Linked Data
ClinVar Variation Id:
1373599
dbSNP Id:
rs756297578
ExAC:
1:2340006 C / T
gnomAD v2:
1-2340006-C-T
gnomAD v3:
1-2408567-C-T
gnomAD v4:
1-2408567-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.2408567C>T , CM000663.2:g.2408567C>T | GRCh38 |
| NC_000001.10:g.2340006C>T , CM000663.1:g.2340006C>T | GRCh37 |
| NC_000001.9:g.2329866C>T | NCBI36 |
| NG_008342.1:g.9005G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000288774.8:c.485G>A | ENSP00000288774.3:p.Arg162Gln | |
| ENST00000447513.7:c.485G>A MANE Select | ENSP00000407922.2:p.Arg162Gln | |
| ENST00000650293.1:c.439G>A | ||
| ENST00000288774.7:c.485G>A | ENSP00000288774.3:p.Arg162Gln | |
| ENST00000447513.6:c.485G>A | ENSP00000407922.2:p.Arg162Gln | |
| ENST00000507596.5:c.485G>A | ENSP00000424291.1:p.Arg162Gln | |
| ENST00000508384.5:c.53G>A | ENSP00000464289.1:p.Arg18Gln | |
| ENST00000510434.1:c.485G>A | ENSP00000423051.1:p.Arg162Gln | |
| NM_002617.3:c.485G>A | NP_002608.1:p.Arg162Gln | |
| NM_153818.1:c.485G>A | NP_722540.1:p.Arg162Gln | |
| XM_011541573.1:c.485G>A | XP_011539875.1:p.Arg162Gln | |
| XM_011541574.1:c.53G>A | XP_011539876.1:p.Arg18Gln | |
| XM_011541575.1:c.53G>A | XP_011539877.1:p.Arg18Gln | |
| XM_011541576.1:c.485G>A | XP_011539878.1:p.Arg162Gln | |
| XR_946666.1:n.605G>A | ||
| XM_011541576.2:c.485G>A | XP_011539878.1:p.Arg162Gln | |
| XR_946666.2:n.554G>A | ||
| NM_001374425.1:c.485G>A | NP_001361354.1:p.Arg162Gln | |
| NM_001374426.1:c.53G>A | NP_001361355.1:p.Arg18Gln | |
| NM_001374427.1:c.53G>A | NP_001361356.1:p.Arg18Gln | |
| NM_002617.4:c.485G>A MANE Select | NP_002608.1:p.Arg162Gln | |
| NM_153818.2:c.485G>A | NP_722540.1:p.Arg162Gln | |
| NR_164636.1:n.604G>A |