Linked Data
ClinVar Variation Id:
185889
ClinVar RCV Id:
RCV000165391
RCV000197495
RCV000420216
RCV001119747
RCV001284030
RCV001356268
RCV004535112
dbSNP Id:
rs371149159
ExAC:
16:23641408 C / T
gnomAD v2:
16-23641408-C-T
gnomAD v3:
16-23630087-C-T
gnomAD v4:
16-23630087-C-T
PubMed:
PMID:26283626
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23630087C>T , CM000678.2:g.23630087C>T | GRCh38 |
| NC_000016.9:g.23641408C>T , CM000678.1:g.23641408C>T | GRCh37 |
| NC_000016.8:g.23548909C>T | NCBI36 |
| NG_007406.1:g.16271G>A , LRG_308:g.16271G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561514.3:c.2073G>A | ENSP00000460666.3:p.Ser691= | |
| ENST00000565038.2:c.212-812G>A | ENSP00000459882.2:n.212-812G>A | |
| ENST00000566069.6:c.2067G>A | ENSP00000459237.2:p.Ser689= | |
| ENST00000697377.2:c.2073G>A | ENSP00000513286.2:p.Ser691= | |
| ENST00000697379.2:c.2073G>A | ENSP00000513287.2:p.Ser691= | |
| ENST00000561514.2:c.1182G>A | ENSP00000460666.2:p.Ser394= | |
| ENST00000697374.1:c.1182G>A | ENSP00000513284.1:p.Ser394= | |
| ENST00000697375.1:n.3414G>A | ||
| ENST00000697376.1:c.1182G>A | ENSP00000513285.1:p.Ser394= | |
| ENST00000697377.1:c.1182G>A | ENSP00000513286.1:p.Ser394= | |
| ENST00000697378.1:n.2587G>A | ||
| ENST00000697379.1:c.1182G>A | ENSP00000513287.1:p.Ser394= | |
| ENST00000697380.1:n.995G>A | ||
| ENST00000697381.1:n.762G>A | ||
| ENST00000697382.1:c.1182G>A | ENSP00000513288.1:p.Ser394= | |
| ENST00000697383.1:c.49-812G>A | ENSP00000513289.1:n.49-812G>A | |
| ENST00000697384.1:n.2221G>A | ||
| ENST00000261584.9:c.2067G>A MANE Select | ENSP00000261584.4:p.Ser689= | |
| ENST00000261584.8:c.2067G>A | ENSP00000261584.4:p.Ser689= | |
| ENST00000565038.1:c.87-812G>A | ||
| ENST00000568219.5:c.1182G>A | ENSP00000454703.2:p.Ser394= | |
| NM_024675.3:c.2067G>A , LRG_308t1:c.2067G>A | NP_078951.2:p.Ser689= | |
| XM_011545946.1:c.2073G>A | XP_011544248.1:p.Ser691= | |
| XM_011545947.1:c.2073G>A | XP_011544249.1:p.Ser691= | |
| XM_011545948.1:c.1182G>A | XP_011544250.1:p.Ser394= | |
| XR_950851.1:n.2863G>A | ||
| XM_011545946.2:c.2073G>A | XP_011544248.1:p.Ser691= | |
| XM_011545947.2:c.2073G>A | XP_011544249.1:p.Ser691= | |
| XM_011545948.2:c.1182G>A | XP_011544250.1:p.Ser394= | |
| XM_017023671.1:c.2073G>A | XP_016879160.1:p.Ser691= | |
| XM_017023672.2:c.2067G>A | XP_016879161.1:p.Ser689= | |
| XM_017023673.2:c.2067G>A | XP_016879162.1:p.Ser689= | |
| NM_024675.4:c.2067G>A MANE Select | NP_078951.2:p.Ser689= |