Linked Data
MyVariant Identifiers:
chr4:g.52894194A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52028028A>C , CM000666.2:g.52028028A>C | GRCh38 |
| NC_000004.11:g.52894194A>C , CM000666.1:g.52894194A>C | GRCh37 |
| NC_000004.10:g.52588951A>C | NCBI36 |
| NG_008891.1:g.15292T>G , LRG_204:g.15292T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000381431.10:c.693T>G MANE Select | ENSP00000370839.6:p.Gly231= | |
| ENST00000381431.9:c.693T>G | ENSP00000370839.5:p.Gly231= | |
| NM_000232.4:c.693T>G , LRG_204t1:c.693T>G | NP_000223.1:p.Gly231= | |
| XM_006714049.2:c.396T>G | XP_006714112.1:p.Gly132= | |
| XM_011534403.1:c.483T>G | XP_011532705.1:p.Gly161= | |
| XM_011534404.1:c.396T>G | XP_011532706.1:p.Gly132= | |
| NM_000232.5:c.693T>G MANE Select | NP_000223.1:p.Gly231= |