Linked Data
ClinVar Variation Id:
2005021
ClinVar RCV Id:
RCV002820714
MyVariant Identifiers:
chr11:g.47463241C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.47441689C>T , CM000673.2:g.47441689C>T | GRCh38 |
| NC_000011.9:g.47463241C>T , CM000673.1:g.47463241C>T | GRCh37 |
| NC_000011.8:g.47419817C>T | NCBI36 |
| NG_008312.1:g.12490G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000298854.7:c.834G>A MANE Select | ENSP00000298854.2:p.Glu278= | |
| ENST00000298854.6:c.834G>A | ENSP00000298854.2:p.Glu278= | |
| ENST00000352508.7:c.789+134G>A | ENSP00000298853.3:n.789+134G>A | |
| ENST00000524487.5:c.675G>A | ENSP00000435551.2:p.Glu225= | |
| ENST00000528356.1:n.43G>A | ||
| ENST00000529341.1:c.789+134G>A | ENSP00000431732.1:n.789+134G>A | |
| NM_005055.4:c.834G>A | NP_005046.2:p.Glu278= | |
| NM_032645.4:c.789+134G>A | NP_116034.2:n.789+134G>A | |
| XM_005253042.2:c.834G>A | XP_005253099.1:p.Glu278= | |
| XM_005253043.2:c.789+134G>A | XP_005253100.1:n.789+134G>A | |
| XM_011520252.1:c.834G>A | XP_011518554.1:p.Glu278= | |
| XM_011520253.1:c.834G>A | XP_011518555.1:p.Glu278= | |
| XM_005253042.3:c.834G>A | XP_005253099.1:p.Glu278= | |
| XM_005253043.3:c.789+134G>A | XP_005253100.1:n.789+134G>A | |
| NM_005055.5:c.834G>A MANE Select | NP_005046.2:p.Glu278= | |
| NM_032645.5:c.789+134G>A | NP_116034.2:n.789+134G>A |