Linked Data
MyVariant Identifiers:
chr4:g.187455404A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186534250A>T , CM000666.2:g.186534250A>T | GRCh38 |
| NC_000004.11:g.187455404A>T , CM000666.1:g.187455404A>T | GRCh37 |
| NC_000004.10:g.187692398A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703170.1:c.492T>A | ENSP00000515216.1:p.Arg164= | |
| ENST00000307161.5:c.492T>A MANE Select | ENSP00000302811.5:p.Arg164= | |
| ENST00000509111.2:c.147+20932T>A | ||
| NM_005958.3:c.492T>A | NP_005949.1:p.Arg164= | |
| XM_011532002.1:c.237T>A | XP_011530304.1:p.Arg79= | |
| XR_939589.1:n.1982-11394A>T | ||
| XR_939590.1:n.162-11394A>T | ||
| NM_005958.4:c.492T>A MANE Select | NP_005949.1:p.Arg164= | |
| XM_011532002.3:c.237T>A | XP_011530304.1:p.Arg79= | |
| XR_939589.2:n.1982-11394A>T | ||
| XR_939590.2:n.162-11394A>T |