Linked Data
ClinVar Variation Id:
1666712
dbSNP Id:
rs764869982
ExAC:
11:111959598 C / T
gnomAD v4:
11-112088874-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112088874C>T , CM000673.2:g.112088874C>T | GRCh38 |
| NC_000011.9:g.111959598C>T , CM000673.1:g.111959598C>T | GRCh37 |
| NC_000011.8:g.111464808C>T | NCBI36 |
| NG_012337.2:g.7028C>T | |
| NG_033145.1:g.2925G>A | |
| NG_012337.3:g.7028C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000530923.6:c.177C>T | ENSP00000432946.2:p.Ser59= | |
| ENST00000534010.2:c.177C>T | ENSP00000433202.2:p.Ser59= | |
| ENST00000375549.8:c.177C>T MANE Select | ENSP00000364699.3:p.Ser59= | |
| ENST00000528021.6:c.177C>T | ENSP00000432465.1:p.Ser59= | |
| ENST00000640554.1:c.*249C>T | ENSP00000491141.1:n.*249C>T | |
| ENST00000375549.7:c.177C>T | ENSP00000364699.3:p.Ser59= | |
| ENST00000525291.5:c.60C>T | ENSP00000436669.1:p.Ser20= | |
| ENST00000525987.5:n.182C>T | ||
| ENST00000526592.5:c.177C>T | ENSP00000432005.1:p.Ser59= | |
| ENST00000528021.5:c.177C>T | ENSP00000432465.1:p.Ser59= | |
| ENST00000528048.5:c.169+901C>T | ENSP00000436217.1:n.169+901C>T | |
| ENST00000528182.5:c.177C>T | ENSP00000435475.1:p.Ser59= | |
| ENST00000530923.5:c.167C>T | ||
| ENST00000531744.5:c.177C>T | ENSP00000456957.1:p.Ser59= | |
| ENST00000532699.1:c.177C>T | ENSP00000456434.1:p.Ser59= | |
| ENST00000534010.1:c.8C>T | ||
| ENST00000614349.4:c.177C>T | ENSP00000480666.1:p.Ser59= | |
| NM_001276503.1:c.169+901C>T | NP_001263432.1:n.169+901C>T | |
| NM_001276504.1:c.60C>T | NP_001263433.1:p.Ser20= | |
| NM_001276506.1:c.177C>T | NP_001263435.1:p.Ser59= | |
| NM_003002.3:c.177C>T | NP_002993.1:p.Ser59= | |
| NR_077060.1:n.261C>T | ||
| NM_003002.4:c.177C>T MANE Select | NP_002993.1:p.Ser59= | |
| NM_001276503.2:c.169+901C>T | NP_001263432.1:n.169+901C>T | |
| NM_001276504.2:c.60C>T | NP_001263433.1:p.Ser20= | |
| NM_001276506.2:c.177C>T | NP_001263435.1:p.Ser59= | |
| NR_077060.2:n.212C>T |