Linked Data
MyVariant Identifiers:
chr4:g.52894241A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52028075A>G , CM000666.2:g.52028075A>G | GRCh38 |
| NC_000004.11:g.52894241A>G , CM000666.1:g.52894241A>G | GRCh37 |
| NC_000004.10:g.52588998A>G | NCBI36 |
| NG_008891.1:g.15245T>C , LRG_204:g.15245T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381431.10:c.646T>C MANE Select | ENSP00000370839.6:p.Leu216= | |
| ENST00000381431.9:c.646T>C | ENSP00000370839.5:p.Leu216= | |
| NM_000232.4:c.646T>C , LRG_204t1:c.646T>C | NP_000223.1:p.Leu216= | |
| XM_006714049.2:c.349T>C | XP_006714112.1:p.Leu117= | |
| XM_011534403.1:c.436T>C | XP_011532705.1:p.Leu146= | |
| XM_011534404.1:c.349T>C | XP_011532706.1:p.Leu117= | |
| NM_000232.5:c.646T>C MANE Select | NP_000223.1:p.Leu216= |