Linked Data
ClinVar Variation Id:
998352
ClinVar RCV Id:
RCV001294174
dbSNP Id:
rs145611597
ExAC:
11:44148399 C / T
gnomAD v2:
11-44148399-C-T
gnomAD v3:
11-44126849-C-T
gnomAD v4:
11-44126849-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.44126849C>T , CM000673.2:g.44126849C>T | GRCh38 |
| NC_000011.9:g.44148399C>T , CM000673.1:g.44148399C>T | GRCh37 |
| NC_000011.8:g.44104975C>T | NCBI36 |
| NG_007560.1:g.36301C>T , LRG_494:g.36301C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343631.4:c.973C>T | ENSP00000342656.3:p.Arg325Trp | |
| ENST00000395673.8:c.973C>T | ENSP00000379032.4:p.Arg325Trp | |
| ENST00000531161.6:n.1132C>T | ||
| ENST00000682359.1:c.939+1865C>T | ENSP00000508226.1:n.939+1865C>T | |
| ENST00000682711.1:c.-544+30997C>T | ENSP00000506803.1:n.-544+30997C>T | |
| ENST00000682815.1:c.973C>T | ENSP00000507234.1:p.Arg325Trp | |
| ENST00000682947.1:n.1147C>T | ||
| ENST00000682993.1:c.973C>T | ENSP00000507580.1:p.Arg325Trp | |
| ENST00000683000.1:c.973C>T | ENSP00000508361.1:p.Arg325Trp | |
| ENST00000683299.1:n.1390C>T | ||
| ENST00000683870.1:c.973C>T | ENSP00000507922.1:p.Arg325Trp | |
| ENST00000683881.1:n.3534C>T | ||
| ENST00000684039.1:c.973C>T | ENSP00000507677.1:p.Arg325Trp | |
| ENST00000684124.1:c.973C>T | ENSP00000508332.1:p.Arg325Trp | |
| ENST00000684533.1:c.744-3196C>T | ENSP00000507915.1:n.744-3196C>T | |
| ENST00000533608.7:c.973C>T MANE Select | ENSP00000431173.2:p.Arg325Trp | |
| ENST00000343631.3:c.973C>T | ENSP00000342656.3:p.Arg325Trp | |
| ENST00000358681.8:c.973C>T | ENSP00000351509.4:p.Arg325Trp | |
| ENST00000395673.7:c.1072C>T | ENSP00000379032.3:p.Arg358Trp | |
| ENST00000531161.5:n.150C>T | ||
| ENST00000533608.5:c.973C>T | ENSP00000431173.1:p.Arg325Trp | |
| NM_000401.3:c.1072C>T , LRG_494t1:c.1072C>T | NP_000392.3:p.Arg358Trp | |
| NM_001178083.1:c.973C>T | NP_001171554.1:p.Arg325Trp | |
| NM_207122.1:c.973C>T , LRG_494t2:c.973C>T | NP_997005.1:p.Arg325Trp | |
| XM_011519950.1:c.1111C>T | XP_011518252.1:p.Arg371Trp | |
| XM_011519951.1:c.1012C>T | XP_011518253.1:p.Arg338Trp | |
| XM_024448383.1:c.1111C>T | XP_024304151.1:p.Arg371Trp | |
| NM_001178083.2:c.973C>T | NP_001171554.1:p.Arg325Trp | |
| NM_207122.2:c.973C>T MANE Select | NP_997005.1:p.Arg325Trp | |
| NM_001178083.3:c.973C>T | NP_001171554.1:p.Arg325Trp | |
| NM_001389628.1:c.973C>T | NP_001376557.1:p.Arg325Trp | |
| NM_001389630.1:c.973C>T | NP_001376559.1:p.Arg325Trp |