Linked Data
MyVariant Identifiers:
chr5:g.71015198T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.71719371T>A , CM000667.2:g.71719371T>A | GRCh38 |
| NC_000005.9:g.71015198T>A , CM000667.1:g.71015198T>A | GRCh37 |
| NC_000005.8:g.71050954T>A | NCBI36 |
| NG_015988.1:g.5209T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296777.5:c.78T>A MANE Select | ENSP00000296777.4:p.Arg26= | |
| ENST00000296777.4:c.78T>A | ENSP00000296777.4:p.Arg26= | |
| NM_004291.3:c.78T>A | NP_004282.1:p.Arg26= | |
| NM_004291.4:c.78T>A MANE Select | NP_004282.1:p.Arg26= |