Linked Data
ClinVar Variation Id:
1539680
ClinVar RCV Id:
RCV002169671
dbSNP Id:
rs2115698584
MyVariant Identifiers:
chr7:g.65547908G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.66082921G>T , CM000669.2:g.66082921G>T | GRCh38 |
| NC_000007.13:g.65547908G>T , CM000669.1:g.65547908G>T | GRCh37 |
| NC_000007.12:g.65185343G>T | NCBI36 |
| NG_009288.1:g.12133G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304874.14:c.333G>T MANE Select | ENSP00000307188.9:p.Arg111= | |
| ENST00000362000.10:c.138G>T | ENSP00000354710.6:p.Arg46= | |
| ENST00000380839.9:c.333G>T | ENSP00000370219.4:p.Arg111= | |
| ENST00000395331.4:c.333G>T | ENSP00000378740.3:p.Arg111= | |
| ENST00000395332.8:c.333G>T | ENSP00000378741.3:p.Arg111= | |
| ENST00000671817.1:c.333G>T | ENSP00000500462.1:p.Arg111= | |
| ENST00000672498.1:c.333G>T | ENSP00000500227.1:p.Arg111= | |
| ENST00000672586.1:n.238G>T | ||
| ENST00000672676.1:n.503G>T | ||
| ENST00000673149.1:n.145G>T | ||
| ENST00000673350.1:n.581G>T | ||
| ENST00000673518.1:c.333G>T | ENSP00000499889.1:p.Arg111= | |
| ENST00000673594.1:n.182G>T | ||
| ENST00000304874.13:c.333G>T | ENSP00000307188.9:p.Arg111= | |
| ENST00000362000.9:c.138G>T | ENSP00000354710.5:p.Arg46= | |
| ENST00000380839.8:c.333G>T | ENSP00000370219.4:p.Arg111= | |
| ENST00000395331.3:c.333G>T | ENSP00000378740.3:p.Arg111= | |
| ENST00000395332.7:c.333G>T | ENSP00000378741.3:p.Arg111= | |
| ENST00000487982.5:n.399G>T | ||
| ENST00000496336.1:n.574G>T | ||
| NM_000048.3:c.333G>T | NP_000039.2:p.Arg111= | |
| NM_001024943.1:c.333G>T | NP_001020114.1:p.Arg111= | |
| NM_001024944.1:c.333G>T | NP_001020115.1:p.Arg111= | |
| NM_001024946.1:c.333G>T | NP_001020117.1:p.Arg111= | |
| NM_000048.4:c.333G>T MANE Select | NP_000039.2:p.Arg111= | |
| NM_001024943.2:c.333G>T | NP_001020114.1:p.Arg111= | |
| NM_001024944.2:c.333G>T | NP_001020115.1:p.Arg111= | |
| NM_001024946.2:c.333G>T | NP_001020117.1:p.Arg111= |