Linked Data
ClinVar Variation Id:
2984621
ClinVar RCV Id:
RCV003845764
MyVariant Identifiers:
chr11:g.88911754T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.89178586T>C , CM000673.2:g.89178586T>C | GRCh38 |
| NC_000011.9:g.88911754T>C , CM000673.1:g.88911754T>C | GRCh37 |
| NC_000011.8:g.88551402T>C | NCBI36 |
| NG_008748.1:g.5715T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263321.6:c.633T>C MANE Select | ENSP00000263321.4:p.His211= | |
| ENST00000263321.5:c.633T>C | ENSP00000263321.4:p.His211= | |
| ENST00000526139.1:n.694T>C | ||
| NM_000372.4:c.633T>C | NP_000363.1:p.His211= | |
| XM_011542970.1:c.633T>C | XP_011541272.1:p.His211= | |
| XM_011542970.2:c.633T>C | XP_011541272.1:p.His211= | |
| XR_001748321.1:n.2718-65053A>G | ||
| XR_001748322.1:n.2733-65053A>G | ||
| NM_000372.5:c.633T>C MANE Select | NP_000363.1:p.His211= |