Linked Data
ClinVar Variation Id:
2751706
ClinVar RCV Id:
RCV003515005
MyVariant Identifiers:
chr16:g.47732421A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.47698510A>G , CM000678.2:g.47698510A>G | GRCh38 |
| NC_000016.9:g.47732421A>G , CM000678.1:g.47732421A>G | GRCh37 |
| NC_000016.8:g.46289922A>G | NCBI36 |
| NG_016598.1:g.242212A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696809.1:c.*1640A>G | ENSP00000512887.1:n.*1640A>G | |
| ENST00000699276.1:c.*694A>G | ENSP00000514257.1:n.*694A>G | |
| ENST00000323584.10:c.3066A>G MANE Select | ENSP00000313504.5:p.Val1022= | |
| ENST00000299167.12:c.3066A>G | ENSP00000299167.8:p.Val1022= | |
| ENST00000323584.9:c.3066A>G | ENSP00000313504.5:p.Val1022= | |
| ENST00000564711.2:c.80A>G | ||
| ENST00000566044.5:c.3045A>G | ENSP00000456729.1:p.Val1015= | |
| ENST00000566319.2:n.1882A>G | ||
| NM_000293.2:c.3066A>G | NP_000284.1:p.Val1022= | |
| NM_001031835.2:c.3045A>G | NP_001027005.1:p.Val1015= | |
| XM_005255983.3:c.3066A>G | XP_005256040.1:p.Val1022= | |
| XM_005255984.3:c.3045A>G | XP_005256041.1:p.Val1015= | |
| XM_011523107.1:c.1644A>G | XP_011521409.1:p.Val548= | |
| NM_001363837.1:c.3066A>G | NP_001350766.1:p.Val1022= | |
| XM_005255983.4:c.3066A>G | XP_005256040.1:p.Val1022= | |
| XM_005255984.4:c.3045A>G | XP_005256041.1:p.Val1015= | |
| XM_017023282.1:c.1953A>G | XP_016878771.1:p.Val651= | |
| XM_017023283.1:c.1644A>G | XP_016878772.1:p.Val548= | |
| XM_017023284.1:c.1644A>G | XP_016878773.1:p.Val548= | |
| XR_001751913.1:n.2990A>G | ||
| NM_000293.3:c.3066A>G MANE Select | NP_000284.1:p.Val1022= | |
| NM_001031835.3:c.3045A>G | NP_001027005.1:p.Val1015= |