Linked Data
ClinVar Variation Id:
2056522
ClinVar RCV Id:
RCV002947520
dbSNP Id:
rs1892921606
MyVariant Identifiers:
chr15:g.66774157C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.66481819C>G , CM000677.2:g.66481819C>G | GRCh38 |
| NC_000015.9:g.66774157C>G , CM000677.1:g.66774157C>G | GRCh37 |
| NC_000015.8:g.64561211C>G | NCBI36 |
| NG_008305.1:g.99947C>G , LRG_725:g.99947C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684779.1:c.567C>G | ENSP00000508681.1:p.Val189= | |
| ENST00000685172.1:c.633C>G | ENSP00000509604.1:p.Val211= | |
| ENST00000685763.1:c.486C>G | ENSP00000509016.1:p.Val162= | |
| ENST00000686347.1:c.569-5409C>G | ENSP00000509027.1:n.569-5409C>G | |
| ENST00000687191.1:n.991C>G | ||
| ENST00000689951.1:c.684C>G | ENSP00000509308.1:p.Val228= | |
| ENST00000691077.1:c.633C>G | ENSP00000509843.1:p.Val211= | |
| ENST00000691576.1:c.569-3175C>G | ENSP00000510066.1:n.569-3175C>G | |
| ENST00000691937.1:c.633C>G | ENSP00000508768.1:p.Val211= | |
| ENST00000692487.1:c.633C>G | ENSP00000509534.1:p.Val211= | |
| ENST00000692683.1:c.567C>G | ENSP00000508437.1:p.Val189= | |
| ENST00000693150.1:c.489C>G | ENSP00000510309.1:p.Val163= | |
| ENST00000307102.10:c.633C>G MANE Select | ENSP00000302486.5:p.Val211= | |
| ENST00000307102.9:c.633C>G | ENSP00000302486.4:p.Val211= | |
| ENST00000566326.1:c.105C>G | ENSP00000456438.1:p.Val35= | |
| NM_002755.3:c.633C>G , LRG_725t1:c.633C>G | NP_002746.1:p.Val211= | |
| XM_011521783.1:c.567C>G | XP_011520085.1:p.Val189= | |
| XM_011521783.3:c.567C>G | XP_011520085.1:p.Val189= | |
| XM_017022411.2:c.555C>G | XP_016877900.1:p.Val185= | |
| XM_017022412.1:c.489C>G | XP_016877901.1:p.Val163= | |
| XM_017022413.1:c.105C>G | XP_016877902.1:p.Val35= | |
| NM_002755.4:c.633C>G MANE Select | NP_002746.1:p.Val211= |