Linked Data
ClinVar Variation Id:
559181
ClinVar RCV Id:
RCV000676340
dbSNP Id:
rs1802834
ExAC:
16:2035999 C / T
gnomAD v2:
16-2035999-C-T
gnomAD v3:
16-1985998-C-T
gnomAD v4:
16-1985998-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1985998C>T , CM000678.2:g.1985998C>T | GRCh38 |
| NC_000016.9:g.2035999C>T , CM000678.1:g.2035999C>T | GRCh37 |
| NC_000016.8:g.1976000C>T | NCBI36 |
| NG_016288.1:g.6850C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567719.2:c.363C>T | ENSP00000455885.1:p.Arg121= | |
| ENST00000248114.7:c.588C>T MANE Select | ENSP00000248114.6:p.Arg196= | |
| ENST00000248114.6:c.588C>T | ENSP00000248114.6:p.Arg196= | |
| ENST00000565658.1:n.745C>T | ||
| ENST00000567719.1:c.363C>T | ENSP00000455885.1:p.Arg121= | |
| ENST00000569451.1:c.*61C>T | ENSP00000456432.1:n.*61C>T | |
| NM_005262.2:c.588C>T | NP_005253.3:p.Arg196= | |
| NM_005262.3:c.588C>T MANE Select | NP_005253.3:p.Arg196= |