Linked Data
ClinVar Variation Id:
2563635
ClinVar RCV Id:
RCV004332260
MyVariant Identifiers:
chr1:g.10384906C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.10324848C>T , CM000663.2:g.10324848C>T | GRCh38 |
| NC_000001.10:g.10384906C>T , CM000663.1:g.10384906C>T | GRCh37 |
| NC_000001.9:g.10307493C>T | NCBI36 |
| NG_008069.1:g.119143C>T , LRG_252:g.119143C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696502.1:c.2490C>T | ENSP00000512668.1:p.Gly830= | |
| ENST00000696503.1:c.2553C>T | ENSP00000512669.1:p.Gly851= | |
| ENST00000696504.1:c.2553C>T | ENSP00000512670.1:p.Gly851= | |
| ENST00000676179.1:c.2628C>T MANE Select | ENSP00000502065.1:p.Gly876= | |
| ENST00000263934.10:c.2490C>T | ENSP00000263934.6:p.Gly830= | |
| ENST00000377081.5:c.2628C>T | ENSP00000366284.1:p.Gly876= | |
| ENST00000377086.5:c.2628C>T | ENSP00000366290.1:p.Gly876= | |
| ENST00000620295.2:c.2586C>T | ENSP00000478500.1:p.Gly862= | |
| ENST00000622724.3:c.2550C>T | ENSP00000480063.1:p.Gly850= | |
| NM_015074.3:c.2490C>T , LRG_252t1:c.2490C>T | NP_055889.2:p.Gly830= | |
| NM_001365951.1:c.2628C>T | NP_001352880.1:p.Gly876= | |
| NM_001365952.1:c.2628C>T | NP_001352881.1:p.Gly876= | |
| NM_001365951.3:c.2628C>T MANE Select | NP_001352880.1:p.Gly876= |