Linked Data
ClinVar Variation Id:
2816114
ClinVar RCV Id:
RCV003607908
COSMIC:
COSM3279836
MyVariant Identifiers:
chr16:g.23641012A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23629691A>G , CM000678.2:g.23629691A>G | GRCh38 |
| NC_000016.9:g.23641012A>G , CM000678.1:g.23641012A>G | GRCh37 |
| NC_000016.8:g.23548513A>G | NCBI36 |
| NG_007406.1:g.16667T>C , LRG_308:g.16667T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561514.3:c.2469T>C | ENSP00000460666.3:p.Asn823= | |
| ENST00000565038.2:c.212-416T>C | ENSP00000459882.2:n.212-416T>C | |
| ENST00000566069.6:c.2463T>C | ENSP00000459237.2:p.Asn821= | |
| ENST00000697377.2:c.2469T>C | ENSP00000513286.2:p.Asn823= | |
| ENST00000697379.2:c.2469T>C | ENSP00000513287.2:p.Asn823= | |
| ENST00000561514.2:c.1578T>C | ENSP00000460666.2:p.Asn526= | |
| ENST00000697374.1:c.1578T>C | ENSP00000513284.1:p.Asn526= | |
| ENST00000697375.1:n.3810T>C | ||
| ENST00000697376.1:c.1578T>C | ENSP00000513285.1:p.Asn526= | |
| ENST00000697377.1:c.1578T>C | ENSP00000513286.1:p.Asn526= | |
| ENST00000697378.1:n.2983T>C | ||
| ENST00000697379.1:c.1578T>C | ENSP00000513287.1:p.Asn526= | |
| ENST00000697380.1:n.1391T>C | ||
| ENST00000697381.1:n.1158T>C | ||
| ENST00000697382.1:c.1578T>C | ENSP00000513288.1:p.Asn526= | |
| ENST00000697383.1:c.49-416T>C | ENSP00000513289.1:n.49-416T>C | |
| ENST00000697384.1:n.2617T>C | ||
| ENST00000261584.9:c.2463T>C MANE Select | ENSP00000261584.4:p.Asn821= | |
| ENST00000261584.8:c.2463T>C | ENSP00000261584.4:p.Asn821= | |
| ENST00000565038.1:c.87-416T>C | ||
| ENST00000568219.5:c.1578T>C | ENSP00000454703.2:p.Asn526= | |
| NM_024675.3:c.2463T>C , LRG_308t1:c.2463T>C | NP_078951.2:p.Asn821= | |
| XM_011545946.1:c.2469T>C | XP_011544248.1:p.Asn823= | |
| XM_011545947.1:c.2469T>C | XP_011544249.1:p.Asn823= | |
| XM_011545948.1:c.1578T>C | XP_011544250.1:p.Asn526= | |
| XR_950851.1:n.3259T>C | ||
| XM_011545946.2:c.2469T>C | XP_011544248.1:p.Asn823= | |
| XM_011545947.2:c.2469T>C | XP_011544249.1:p.Asn823= | |
| XM_011545948.2:c.1578T>C | XP_011544250.1:p.Asn526= | |
| XM_017023671.1:c.2469T>C | XP_016879160.1:p.Asn823= | |
| XM_017023672.2:c.2463T>C | XP_016879161.1:p.Asn821= | |
| XM_017023673.2:c.2463T>C | XP_016879162.1:p.Asn821= | |
| NM_024675.4:c.2463T>C MANE Select | NP_078951.2:p.Asn821= |