Linked Data
ClinVar Variation Id:
1558580
ClinVar RCV Id:
RCV002200026
dbSNP Id:
rs2138656172
MyVariant Identifiers:
chr14:g.23890191C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23420982C>G , CM000676.2:g.23420982C>G | GRCh38 |
| NC_000014.8:g.23890191C>G , CM000676.1:g.23890191C>G | GRCh37 |
| NC_000014.7:g.22960031C>G | NCBI36 |
| NG_007884.1:g.19680G>C , LRG_384:g.19680G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.3312G>C MANE Select | ENSP00000347507.3:p.Leu1104= | |
| ENST00000355349.3:c.3312G>C | ENSP00000347507.3:p.Leu1104= | |
| NM_000257.3:c.3312G>C | NP_000248.2:p.Leu1104= | |
| XR_245686.3:n.3420G>C | ||
| XM_017021340.1:c.3312G>C | XP_016876829.1:p.Leu1104= | |
| NM_000257.4:c.3312G>C MANE Select | NP_000248.2:p.Leu1104= |