Linked Data
ClinVar Variation Id:
2570622
ClinVar RCV Id:
RCV003307382
MyVariant Identifiers:
chr1:g.171621284C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171652144C>T , CM000663.2:g.171652144C>T | GRCh38 |
| NC_000001.10:g.171621284C>T , CM000663.1:g.171621284C>T | GRCh37 |
| NC_000001.9:g.169887907C>T | NCBI36 |
| NG_008859.1:g.5490G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.468G>A MANE Select | ENSP00000037502.5:p.Lys156= | |
| ENST00000638471.1:c.130+338G>A | ENSP00000491206.1:n.130+338G>A | |
| ENST00000037502.10:c.468G>A | ENSP00000037502.5:p.Lys156= | |
| ENST00000614688.1:c.468G>A | ENSP00000478680.1:p.Lys156= | |
| NM_000261.1:c.468G>A | NP_000252.1:p.Lys156= | |
| NM_000261.2:c.468G>A MANE Select | NP_000252.1:p.Lys156= |