Linked Data
ClinVar Variation Id:
2544995
ClinVar RCV Id:
RCV004314754
dbSNP Id:
rs368684879
ExAC:
4:184210594 C / T
gnomAD v2:
4-184210594-C-T
gnomAD v3:
4-183289441-C-T
gnomAD v4:
4-183289441-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.183289441C>T , CM000666.2:g.183289441C>T | GRCh38 |
| NC_000004.11:g.184210594C>T , CM000666.1:g.184210594C>T | GRCh37 |
| NC_000004.10:g.184447588C>T | NCBI36 |
| NG_051586.1:g.195807C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000403733.8:c.3190C>T MANE Select | ENSP00000384222.3:p.Arg1064Trp | |
| ENST00000403733.7:c.3190C>T | ENSP00000384222.3:p.Arg1064Trp | |
| ENST00000427431.5:c.*2582C>T | ENSP00000393342.1:n.*2582C>T | |
| ENST00000438543.5:c.*986C>T | ENSP00000413521.1:n.*986C>T | |
| ENST00000448232.6:c.3262C>T | ENSP00000398577.2:p.Arg1088Trp | |
| ENST00000504005.5:c.2236C>T | ENSP00000427569.1:p.Arg746Trp | |
| ENST00000508747.1:c.574C>T | ENSP00000420835.1:p.Arg192Trp | |
| ENST00000513834.5:c.3043C>T | ENSP00000425054.1:p.Arg1015Trp | |
| NM_024949.5:c.3190C>T | NP_079225.5:p.Arg1064Trp | |
| XM_011532269.1:c.3262C>T | XP_011530571.1:p.Arg1088Trp | |
| XM_011532269.3:c.3262C>T | XP_011530571.1:p.Arg1088Trp | |
| XM_024454225.1:c.2968C>T | XP_024309993.1:p.Arg990Trp | |
| NM_024949.6:c.3190C>T MANE Select | NP_079225.5:p.Arg1064Trp |