Linked Data
ClinVar Variation Id:
797895
ClinVar RCV Id:
RCV000981377
dbSNP Id:
rs1595086770
MyVariant Identifiers:
chr14:g.23898215T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23429006T>C , CM000676.2:g.23429006T>C | GRCh38 |
| NC_000014.8:g.23898215T>C , CM000676.1:g.23898215T>C | GRCh37 |
| NC_000014.7:g.22968055T>C | NCBI36 |
| NG_007884.1:g.11656A>G , LRG_384:g.11656A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.1356A>G MANE Select | ENSP00000347507.3:p.Pro452= | |
| ENST00000355349.3:c.1356A>G | ENSP00000347507.3:p.Pro452= | |
| NM_000257.3:c.1356A>G | NP_000248.2:p.Pro452= | |
| XR_245686.3:n.1462A>G | ||
| XM_017021340.1:c.1356A>G | XP_016876829.1:p.Pro452= | |
| NM_000257.4:c.1356A>G MANE Select | NP_000248.2:p.Pro452= |