Linked Data
ClinVar Variation Id:
2815783
ClinVar RCV Id:
RCV003685599
MyVariant Identifiers:
chr13:g.20763553C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.20189414C>T , CM000675.2:g.20189414C>T | GRCh38 |
| NC_000013.10:g.20763553C>T , CM000675.1:g.20763553C>T | GRCh37 |
| NC_000013.9:g.19661553C>T | NCBI36 |
| NG_008358.1:g.8562G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000382844.2:c.168G>A | ENSP00000372295.1:p.Leu56= | |
| ENST00000382848.5:c.168G>A MANE Select | ENSP00000372299.4:p.Leu56= | |
| ENST00000382844.1:c.168G>A | ENSP00000372295.1:p.Leu56= | |
| ENST00000382848.4:c.168G>A | ENSP00000372299.4:p.Leu56= | |
| NM_004004.5:c.168G>A | NP_003995.2:p.Leu56= | |
| XM_011535049.1:c.168G>A | XP_011533351.1:p.Leu56= | |
| XM_011535049.2:c.168G>A | XP_011533351.1:p.Leu56= | |
| NM_004004.6:c.168G>A MANE Select | NP_003995.2:p.Leu56= |