Linked Data
ClinVar Variation Id:
2041487
ClinVar RCV Id:
RCV002903007
dbSNP Id:
rs1736090292
MyVariant Identifiers:
chr4:g.187115745T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186194591T>C , CM000666.2:g.186194591T>C | GRCh38 |
| NC_000004.11:g.187115745T>C , CM000666.1:g.187115745T>C | GRCh37 |
| NC_000004.10:g.187352739T>C | NCBI36 |
| NG_007965.1:g.8072T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378802.5:c.306T>C MANE Select | ENSP00000368079.4:p.Leu102= | |
| ENST00000378802.4:c.306T>C | ENSP00000368079.4:p.Leu102= | |
| NM_207352.3:c.306T>C | NP_997235.3:p.Leu102= | |
| XM_005262935.2:c.306T>C | XP_005262992.1:p.Leu102= | |
| XM_006714184.2:c.-5T>C | XP_006714247.1:n.-5T>C | |
| XM_005262935.4:c.306T>C | XP_005262992.1:p.Leu102= | |
| XM_017008037.1:c.-5T>C | XP_016863526.1:n.-5T>C | |
| NM_207352.4:c.306T>C MANE Select | NP_997235.3:p.Leu102= |