Linked Data
ClinVar Variation Id:
2022606
ClinVar RCV Id:
RCV002852611
MyVariant Identifiers:
chr1:g.169454951C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169485713C>A , CM000663.2:g.169485713C>A | GRCh38 |
| NC_000001.10:g.169454951C>A , CM000663.1:g.169454951C>A | GRCh37 |
| NC_000001.9:g.167721575C>A | NCBI36 |
| NG_008255.1:g.5258G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000236137.10:c.54G>T MANE Select | ENSP00000236137.5:p.Val18= | |
| ENST00000646596.1:c.54G>T | ENSP00000494404.1:p.Val18= | |
| ENST00000236137.9:c.54G>T | ENSP00000236137.5:p.Val18= | |
| ENST00000367804.4:c.54G>T | ENSP00000356778.3:p.Val18= | |
| NM_006996.2:c.54G>T | NP_008927.1:p.Val18= | |
| XM_011509076.1:c.12+340G>T | XP_011507378.1:n.12+340G>T | |
| XM_011509077.1:c.54G>T | XP_011507379.1:p.Val18= | |
| NM_001319667.1:c.54G>T | NP_001306596.1:p.Val18= | |
| NM_006996.3:c.54G>T MANE Select | NP_008927.1:p.Val18= |