Linked Data
ClinVar Variation Id:
2098497
ClinVar RCV Id:
RCV003030982
MyVariant Identifiers:
chr13:g.110822940C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.110170593C>T , CM000675.2:g.110170593C>T | GRCh38 |
| NC_000013.10:g.110822940C>T , CM000675.1:g.110822940C>T | GRCh37 |
| NC_000013.9:g.109620941C>T | NCBI36 |
| NG_011544.2:g.141557G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375820.10:c.3696G>A MANE Select | ENSP00000364979.4:p.Glu1232= | |
| ENST00000375820.8:c.3696G>A | ENSP00000364979.4:p.Glu1232= | |
| NM_001845.5:c.3696G>A | NP_001836.3:p.Glu1232= | |
| XM_011521048.1:c.3504G>A | XP_011519350.1:p.Glu1168= | |
| XM_011521048.2:c.3504G>A | XP_011519350.1:p.Glu1168= | |
| NM_001845.6:c.3696G>A MANE Select | NP_001836.3:p.Glu1232= |