Linked Data
ClinVar Variation Id:
1758014
ClinVar RCV Id:
RCV002382589
gnomAD v4:
16-68810235-T-C
MyVariant Identifiers:
chr16:g.68844138T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68810235T>C , CM000678.2:g.68810235T>C | GRCh38 |
| NC_000016.9:g.68844138T>C , CM000678.1:g.68844138T>C | GRCh37 |
| NC_000016.8:g.67401639T>C | NCBI36 |
| NG_008021.1:g.77944T>C , LRG_301:g.77944T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261769.10:c.726T>C MANE Select | ENSP00000261769.4:p.Val242= | |
| ENST00000261769.9:c.726T>C | ENSP00000261769.4:p.Val242= | |
| ENST00000422392.6:c.726T>C | ENSP00000414946.2:p.Val242= | |
| ENST00000561751.1:c.454+1387T>C | ||
| ENST00000562836.5:n.797T>C | ||
| ENST00000566510.5:c.570T>C | ENSP00000458139.1:p.Val190= | |
| ENST00000566612.5:c.726T>C | ENSP00000454782.1:p.Val242= | |
| ENST00000611625.4:c.726T>C | ENSP00000481063.1:p.Val242= | |
| ENST00000612417.4:c.726T>C | ENSP00000478360.1:p.Val242= | |
| ENST00000621016.4:c.726T>C | ENSP00000480664.1:p.Val242= | |
| NM_004360.3:c.726T>C , LRG_301t1:c.726T>C | NP_004351.1:p.Val242= | |
| XM_011523488.1:c.-10T>C | XP_011521790.1:n.-10T>C | |
| XM_011523489.1:c.-10T>C | XP_011521791.1:n.-10T>C | |
| NM_001317184.1:c.726T>C | NP_001304113.1:p.Val242= | |
| NM_001317185.1:c.-890T>C | NP_001304114.1:n.-890T>C | |
| NM_001317186.1:c.-1094T>C | NP_001304115.1:n.-1094T>C | |
| NM_004360.4:c.726T>C | NP_004351.1:p.Val242= | |
| NM_004360.5:c.726T>C MANE Select | NP_004351.1:p.Val242= | |
| NM_001317184.2:c.726T>C | NP_001304113.1:p.Val242= | |
| NM_001317185.2:c.-890T>C | NP_001304114.1:n.-890T>C | |
| NM_001317186.2:c.-1094T>C | NP_001304115.1:n.-1094T>C |