Linked Data
ClinVar Variation Id:
2956018
ClinVar RCV Id:
RCV003813754
dbSNP Id:
rs746735806
ExAC:
16:1412551 G / A
gnomAD v2:
16-1412551-G-A
gnomAD v4:
16-1362550-G-A
MyVariant Identifiers:
chr16:g.1412551G>A (hg19)
chr16:g.1412551_1412561delinsAGGTGGCCCCT (hg19)
chr16:g.1362550G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1362550G>A , CM000678.2:g.1362550G>A | GRCh38 |
| NC_000016.9:g.1412551G>A , CM000678.1:g.1412551G>A | GRCh37 |
| NC_000016.8:g.1352552G>A | NCBI36 |
| NG_016985.1:g.15652G>A | |
| NG_033129.1:g.57155C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000527168.6:n.708+16G>A | ||
| ENST00000529110.2:c.693+16G>A | ENSP00000435349.2:n.693+16G>A | |
| ENST00000529957.6:n.667+16G>A | ||
| ENST00000683366.1:c.*341+16G>A | ENSP00000507283.1:n.*341+16G>A | |
| ENST00000683887.1:c.657+16G>A | ENSP00000506886.1:n.657+16G>A | |
| ENST00000684100.1:n.603+16G>A | ||
| ENST00000684126.1:n.683G>A | ||
| ENST00000684688.1:n.1234+16G>A | ||
| ENST00000204679.9:c.609+16G>A MANE Select | ENSP00000204679.4:n.609+16G>A | |
| ENST00000204679.8:c.609+16G>A | ENSP00000204679.4:n.609+16G>A | |
| ENST00000527076.1:n.1772G>A | ||
| ENST00000527168.5:n.776+16G>A | ||
| ENST00000529957.5:n.708+16G>A | ||
| NM_032520.4:c.609+16G>A | NP_115909.1:n.609+16G>A | |
| XM_017023782.1:c.657+16G>A | XP_016879271.1:n.657+16G>A | |
| XM_017023783.1:c.249+16G>A | XP_016879272.1:n.249+16G>A | |
| NM_032520.5:c.609+16G>A MANE Select | NP_115909.1:n.609+16G>A |