Linked Data
ClinVar Variation Id:
1134324
ClinVar RCV Id:
RCV001469168
dbSNP Id:
rs587776527
MyVariant Identifiers:
chr16:g.23619279G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23607958G>T , CM000678.2:g.23607958G>T | GRCh38 |
| NC_000016.9:g.23619279G>T , CM000678.1:g.23619279G>T | GRCh37 |
| NC_000016.8:g.23526780G>T | NCBI36 |
| NG_007406.1:g.38400C>A , LRG_308:g.38400C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000561514.3:c.3262C>A | ENSP00000460666.3:p.Arg1088= | |
| ENST00000565038.2:c.*737C>A | ENSP00000459882.2:n.*737C>A | |
| ENST00000566069.6:c.3202-4289C>A | ENSP00000459237.2:n.3202-4289C>A | |
| ENST00000697377.2:c.3100C>A | ENSP00000513286.2:p.Arg1034= | |
| ENST00000697379.2:c.3262C>A | ENSP00000513287.2:p.Arg1088= | |
| ENST00000561514.2:c.2371C>A | ENSP00000460666.2:p.Arg791= | |
| ENST00000697374.1:c.2371C>A | ENSP00000513284.1:p.Arg791= | |
| ENST00000697375.1:n.4603C>A | ||
| ENST00000697376.1:c.2317-4289C>A | ENSP00000513285.1:n.2317-4289C>A | |
| ENST00000697377.1:c.2209C>A | ENSP00000513286.1:p.Arg737= | |
| ENST00000697378.1:n.3776C>A | ||
| ENST00000697379.1:c.2371C>A | ENSP00000513287.1:p.Arg791= | |
| ENST00000697380.1:n.2460C>A | ||
| ENST00000697381.1:n.1951C>A | ||
| ENST00000697382.1:c.*33C>A | ENSP00000513288.1:n.*33C>A | |
| ENST00000697383.1:c.790C>A | ENSP00000513289.1:p.Arg264= | |
| ENST00000261584.9:c.3256C>A MANE Select | ENSP00000261584.4:p.Arg1086= | |
| ENST00000261584.8:c.3256C>A | ENSP00000261584.4:p.Arg1086= | |
| ENST00000566069.5:c.117-4289C>A | ||
| ENST00000568219.5:c.2371C>A | ENSP00000454703.2:p.Arg791= | |
| NM_024675.3:c.3256C>A , LRG_308t1:c.3256C>A | NP_078951.2:p.Arg1086= | |
| XM_011545946.1:c.3262C>A | XP_011544248.1:p.Arg1088= | |
| XM_011545947.1:c.3208-4289C>A | XP_011544249.1:n.3208-4289C>A | |
| XM_011545948.1:c.2371C>A | XP_011544250.1:p.Arg791= | |
| XR_950851.1:n.3964C>A | ||
| XM_011545946.2:c.3262C>A | XP_011544248.1:p.Arg1088= | |
| XM_011545947.2:c.3208-4289C>A | XP_011544249.1:n.3208-4289C>A | |
| XM_011545948.2:c.2371C>A | XP_011544250.1:p.Arg791= | |
| XM_017023671.1:c.3120-4289C>A | XP_016879160.1:n.3120-4289C>A | |
| XM_017023672.2:c.3114-4289C>A | XP_016879161.1:n.3114-4289C>A | |
| XM_017023673.2:c.3202-4289C>A | XP_016879162.1:n.3202-4289C>A | |
| NM_024675.4:c.3256C>A MANE Select | NP_078951.2:p.Arg1086= |