Linked Data
ClinVar Variation Id:
1084533
ClinVar RCV Id:
RCV001401605
dbSNP Id:
rs1959063254
MyVariant Identifiers:
chr13:g.20763670G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.20189531G>T , CM000675.2:g.20189531G>T | GRCh38 |
| NC_000013.10:g.20763670G>T , CM000675.1:g.20763670G>T | GRCh37 |
| NC_000013.9:g.19661670G>T | NCBI36 |
| NG_008358.1:g.8445C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000382844.2:c.51C>A | ENSP00000372295.1:p.Ser17= | |
| ENST00000382848.5:c.51C>A MANE Select | ENSP00000372299.4:p.Ser17= | |
| ENST00000382844.1:c.51C>A | ENSP00000372295.1:p.Ser17= | |
| ENST00000382848.4:c.51C>A | ENSP00000372299.4:p.Ser17= | |
| NM_004004.5:c.51C>A | NP_003995.2:p.Ser17= | |
| XM_011535049.1:c.51C>A | XP_011533351.1:p.Ser17= | |
| XM_011535049.2:c.51C>A | XP_011533351.1:p.Ser17= | |
| NM_004004.6:c.51C>A MANE Select | NP_003995.2:p.Ser17= |