Linked Data
MyVariant Identifiers:
chr4:g.42964962T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.42962945T>G , CM000666.2:g.42962945T>G | GRCh38 |
| NC_000004.11:g.42964962T>G , CM000666.1:g.42964962T>G | GRCh37 |
| NC_000004.10:g.42659719T>G | NCBI36 |
| NG_027718.1:g.74680T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000399770.3:c.438T>G MANE Select | ENSP00000382670.2:p.Leu146= | |
| ENST00000399770.2:c.438T>G | ENSP00000382670.2:p.Leu146= | |
| NM_001080476.2:c.438T>G | NP_001073945.1:p.Leu146= | |
| XM_011513691.1:c.75T>G | XP_011511993.1:p.Leu25= | |
| NM_001080476.3:c.438T>G MANE Select | NP_001073945.1:p.Leu146= |