Linked Data
MyVariant Identifiers:
chr3:g.147131191T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.147413404T>A , CM000665.2:g.147413404T>A | GRCh38 |
| NC_000003.11:g.147131191T>A , CM000665.1:g.147131191T>A | GRCh37 |
| NC_000003.10:g.148613881T>A | NCBI36 |
| NG_015886.1:g.9011T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282928.5:c.1197T>A MANE Select | ENSP00000282928.4:p.Ser399= | |
| ENST00000282928.4:c.1197T>A | ENSP00000282928.4:p.Ser399= | |
| ENST00000472523.1:n.521+19462T>A | ||
| ENST00000488404.5:c.263T>A | ||
| NM_003412.3:c.1197T>A | NP_003403.2:p.Ser399= | |
| NM_003412.4:c.1197T>A MANE Select | NP_003403.2:p.Ser399= |