Linked Data
MyVariant Identifiers:
chr4:g.52894260G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52028094G>C , CM000666.2:g.52028094G>C | GRCh38 |
| NC_000004.11:g.52894260G>C , CM000666.1:g.52894260G>C | GRCh37 |
| NC_000004.10:g.52589017G>C | NCBI36 |
| NG_008891.1:g.15226C>G , LRG_204:g.15226C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381431.10:c.627C>G MANE Select | ENSP00000370839.6:p.Thr209= | |
| ENST00000381431.9:c.627C>G | ENSP00000370839.5:p.Thr209= | |
| NM_000232.4:c.627C>G , LRG_204t1:c.627C>G | NP_000223.1:p.Thr209= | |
| XM_006714049.2:c.330C>G | XP_006714112.1:p.Thr110= | |
| XM_011534403.1:c.417C>G | XP_011532705.1:p.Thr139= | |
| XM_011534404.1:c.330C>G | XP_011532706.1:p.Thr110= | |
| NM_000232.5:c.627C>G MANE Select | NP_000223.1:p.Thr209= |