Linked Data
MyVariant Identifiers:
chr3:g.190122600T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190404811T>A , CM000665.2:g.190404811T>A | GRCh38 |
| NC_000003.11:g.190122600T>A , CM000665.1:g.190122600T>A | GRCh37 |
| NC_000003.10:g.191605294T>A | NCBI36 |
| NG_008149.1:g.21760T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264734.3:c.267T>A MANE Select | ENSP00000264734.3:p.Ala89= | |
| ENST00000456423.2:c.115-5092T>A | ENSP00000414136.2:n.115-5092T>A | |
| ENST00000264734.2:c.477T>A | ENSP00000264734.2:p.Ala159= | |
| ENST00000456423.1:c.325-5092T>A | ENSP00000414136.1:n.325-5092T>A | |
| ENST00000468220.1:n.459T>A | ||
| NM_006580.3:c.477T>A | NP_006571.1:p.Ala159= | |
| NM_001378492.1:c.267T>A | NP_001365421.1:p.Ala89= | |
| NM_001378493.1:c.267T>A | NP_001365422.1:p.Ala89= | |
| NM_006580.4:c.267T>A MANE Select | NP_006571.2:p.Ala89= |