Linked Data
MyVariant Identifiers:
chr4:g.52894203T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52028037T>A , CM000666.2:g.52028037T>A | GRCh38 |
| NC_000004.11:g.52894203T>A , CM000666.1:g.52894203T>A | GRCh37 |
| NC_000004.10:g.52588960T>A | NCBI36 |
| NG_008891.1:g.15283A>T , LRG_204:g.15283A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381431.10:c.684A>T MANE Select | ENSP00000370839.6:p.Gly228= | |
| ENST00000381431.9:c.684A>T | ENSP00000370839.5:p.Gly228= | |
| NM_000232.4:c.684A>T , LRG_204t1:c.684A>T | NP_000223.1:p.Gly228= | |
| XM_006714049.2:c.387A>T | XP_006714112.1:p.Gly129= | |
| XM_011534403.1:c.474A>T | XP_011532705.1:p.Gly158= | |
| XM_011534404.1:c.387A>T | XP_011532706.1:p.Gly129= | |
| NM_000232.5:c.684A>T MANE Select | NP_000223.1:p.Gly228= |