Linked Data
MyVariant Identifiers:
chr4:g.4862007A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.4860280A>T , CM000666.2:g.4860280A>T | GRCh38 |
| NC_000004.11:g.4862007A>T , CM000666.1:g.4862007A>T | GRCh37 |
| NC_000004.10:g.4912908A>T | NCBI36 |
| NG_008121.1:g.5616A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382723.5:c.381A>T MANE Select | ENSP00000372170.4:p.Pro127= | |
| ENST00000382723.4:c.381A>T | ENSP00000372170.4:p.Pro127= | |
| NM_002448.3:c.381A>T MANE Select | NP_002439.2:p.Pro127= |