Linked Data
ClinVar Variation Id:
3226911
ClinVar RCV Id:
RCV004522077
MyVariant Identifiers:
chr10:g.48413959G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.47325403C>T , CM000672.2:g.47325403C>T | GRCh38 |
| NC_000010.10:g.48413959G>A , CM000672.1:g.48413959G>A | GRCh37 |
| NC_000010.9:g.48033965G>A | NCBI36 |
| NG_033916.1:g.7914C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000581492.3:c.909C>T MANE Select | ENSP00000463051.1:p.Asp303= | |
| ENST00000581492.2:c.909C>T | ENSP00000463051.1:p.Asp303= | |
| NM_016204.2:c.909C>T | NP_057288.1:p.Asp303= | |
| XM_006717761.2:c.909C>T | XP_006717824.1:p.Asp303= | |
| NM_016204.3:c.909C>T | NP_057288.1:p.Asp303= | |
| NM_016204.4:c.909C>T MANE Select | NP_057288.1:p.Asp303= |