Linked Data
MyVariant Identifiers:
chr4:g.187126365A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186205211A>C , CM000666.2:g.186205211A>C | GRCh38 |
| NC_000004.11:g.187126365A>C , CM000666.1:g.187126365A>C | GRCh37 |
| NC_000004.10:g.187363359A>C | NCBI36 |
| NG_007965.1:g.18692A>C | |
| NG_012095.2:g.1233A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378802.5:c.999A>C MANE Select | ENSP00000368079.4:p.Thr333= | |
| ENST00000378802.4:c.999A>C | ENSP00000368079.4:p.Thr333= | |
| ENST00000502665.1:n.234A>C | ||
| ENST00000507209.5:n.5697A>C | ||
| ENST00000513354.5:n.89A>C | ||
| NM_207352.3:c.999A>C | NP_997235.3:p.Thr333= | |
| XM_005262935.2:c.999A>C | XP_005262992.1:p.Thr333= | |
| XM_006714184.2:c.603A>C | XP_006714247.1:p.Thr201= | |
| XM_005262935.4:c.999A>C | XP_005262992.1:p.Thr333= | |
| XM_017008037.1:c.603A>C | XP_016863526.1:p.Thr201= | |
| NM_207352.4:c.999A>C MANE Select | NP_997235.3:p.Thr333= |