Linked Data
ClinVar Variation Id:
2012805
ClinVar RCV Id:
RCV002843384
gnomAD v4:
16-30186846-C-T
MyVariant Identifiers:
chr16:g.30198167C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.30186846C>T , CM000678.2:g.30186846C>T | GRCh38 |
| NC_000016.9:g.30198167C>T , CM000678.1:g.30198167C>T | GRCh37 |
| NC_000016.8:g.30105668C>T | NCBI36 |
| NG_023415.1:g.8242C>T , LRG_195:g.8242C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696217.1:n.433C>T | ||
| ENST00000219150.10:c.352C>T MANE Select | ENSP00000219150.6:p.Leu118= | |
| ENST00000219150.9:c.352C>T | ENSP00000219150.5:p.Leu118= | |
| ENST00000561815.5:c.460C>T | ENSP00000456756.1:p.Leu154= | |
| ENST00000563778.5:c.352C>T | ENSP00000456266.1:p.Leu118= | |
| ENST00000564768.1:n.165C>T | ||
| ENST00000565497.5:c.352C>T | ENSP00000456457.1:p.Leu118= | |
| ENST00000567034.5:n.820C>T | ||
| ENST00000568763.1:n.1664C>T | ||
| ENST00000568982.5:n.470C>T | ||
| ENST00000569203.5:c.352C>T | ENSP00000454752.1:p.Leu118= | |
| ENST00000569469.1:n.431+126C>T | ||
| ENST00000569970.1:c.352C>T | ENSP00000457509.1:p.Leu118= | |
| ENST00000570045.5:c.352C>T | ENSP00000455552.1:p.Leu118= | |
| ENST00000570244.5:c.229C>T | ENSP00000457332.1:p.Leu77= | |
| NM_001193333.2:c.352C>T | NP_001180262.1:p.Leu118= | |
| NM_007074.3:c.352C>T | NP_009005.1:p.Leu118= | |
| XM_011545714.1:c.352C>T | XP_011544016.1:p.Leu118= | |
| XM_011545714.2:c.352C>T | XP_011544016.1:p.Leu118= | |
| XM_017022885.2:c.352C>T | XP_016878374.1:p.Leu118= | |
| XM_017022886.1:c.352C>T | XP_016878375.1:p.Leu118= | |
| NM_007074.4:c.352C>T MANE Select | NP_009005.1:p.Leu118= | |
| NM_001193333.3:c.352C>T | NP_001180262.1:p.Leu118= |