Linked Data
ClinVar Variation Id:
1513
dbSNP Id:
rs116100695
ExAC:
1:155261709 G / A
gnomAD v2:
1-155261709-G-A
gnomAD v3:
1-155291918-G-A
gnomAD v4:
1-155291918-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.155291918G>A , CM000663.2:g.155291918G>A | GRCh38 |
| NC_000001.10:g.155261709G>A , CM000663.1:g.155261709G>A | GRCh37 |
| NC_000001.9:g.153528333G>A | NCBI36 |
| NG_011677.1:g.14517C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000342741.6:c.1456C>T MANE Select | ENSP00000339933.4:p.Arg486Trp | |
| ENST00000342741.4:c.1456C>T | ENSP00000339933.4:p.Arg486Trp | |
| ENST00000392414.7:c.1363C>T | ENSP00000376214.3:p.Arg455Trp | |
| NM_000298.5:c.1456C>T | NP_000289.1:p.Arg486Trp | |
| NM_181871.3:c.1363C>T | NP_870986.1:p.Arg455Trp | |
| XM_005245266.3:c.1615C>T | XP_005245323.1:p.Arg539Trp | |
| XM_006711386.2:c.1264C>T | XP_006711449.1:p.Arg422Trp | |
| XM_011509640.1:c.1264C>T | XP_011507942.1:p.Arg422Trp | |
| NM_000298.6:c.1456C>T MANE Select | NP_000289.1:p.Arg486Trp | |
| XM_006711386.4:c.1264C>T | XP_006711449.1:p.Arg422Trp | |
| XM_011509640.3:c.1264C>T | XP_011507942.1:p.Arg422Trp | |
| NM_181871.4:c.1363C>T | NP_870986.1:p.Arg455Trp |