Linked Data
ClinVar Variation Id:
756460
ClinVar RCV Id:
RCV000933962
dbSNP Id:
rs567294014
ExAC:
11:17574967 C / T
gnomAD v2:
11-17574967-C-T
gnomAD v3:
11-17553420-C-T
gnomAD v4:
11-17553420-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.17553420C>T , CM000673.2:g.17553420C>T | GRCh38 |
| NC_000011.9:g.17574967C>T , CM000673.1:g.17574967C>T | GRCh37 |
| NC_000011.8:g.17531543C>T | NCBI36 |
| NG_033191.1:g.11048C>T | |
| NG_033191.2:g.11048C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000399391.7:c.477C>T | ENSP00000382323.2:p.His159= | |
| ENST00000399397.6:c.441C>T MANE Select | ENSP00000382329.2:p.His147= | |
| ENST00000399391.6:c.477C>T | ENSP00000382323.2:p.His159= | |
| ENST00000399397.5:c.441C>T | ENSP00000382329.2:p.His147= | |
| ENST00000428619.1:c.258C>T | ENSP00000399057.2:p.His86= | |
| ENST00000498332.5:n.347C>T | ||
| NM_001277269.1:c.477C>T | NP_001264198.1:p.His159= | |
| NM_001292063.1:c.441C>T | NP_001278992.1:p.His147= | |
| NM_001277269.2:c.477C>T | NP_001264198.1:p.His159= | |
| NM_001292063.2:c.441C>T MANE Select | NP_001278992.1:p.His147= |