Linked Data
MyVariant Identifiers:
chr4:g.187120129T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186198975T>C , CM000666.2:g.186198975T>C | GRCh38 |
| NC_000004.11:g.187120129T>C , CM000666.1:g.187120129T>C | GRCh37 |
| NC_000004.10:g.187357123T>C | NCBI36 |
| NG_007965.1:g.12456T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378802.5:c.693T>C MANE Select | ENSP00000368079.4:p.Phe231= | |
| ENST00000378802.4:c.693T>C | ENSP00000368079.4:p.Phe231= | |
| ENST00000507209.5:n.1534T>C | ||
| NM_207352.3:c.693T>C | NP_997235.3:p.Phe231= | |
| XM_005262935.2:c.693T>C | XP_005262992.1:p.Phe231= | |
| XM_006714184.2:c.297T>C | XP_006714247.1:p.Phe99= | |
| XM_005262935.4:c.693T>C | XP_005262992.1:p.Phe231= | |
| XM_017008037.1:c.297T>C | XP_016863526.1:p.Phe99= | |
| NM_207352.4:c.693T>C MANE Select | NP_997235.3:p.Phe231= |