Linked Data
MyVariant Identifiers:
chr3:g.190105938A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190388149A>C , CM000665.2:g.190388149A>C | GRCh38 |
| NC_000003.11:g.190105938A>C , CM000665.1:g.190105938A>C | GRCh37 |
| NC_000003.10:g.191588632A>C | NCBI36 |
| NG_008149.1:g.5098A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000456423.2:c.-181A>C | ENSP00000414136.2:n.-181A>C | |
| ENST00000264734.2:c.30A>C | ENSP00000264734.2:p.Thr10= | |
| ENST00000456423.1:c.30A>C | ENSP00000414136.1:p.Thr10= | |
| ENST00000468220.1:n.306+13546A>C | ||
| NM_006580.3:c.30A>C | NP_006571.1:p.Thr10= | |
| NM_001378492.1:c.-93-88A>C | NP_001365421.1:n.-93-88A>C | |
| NM_001378493.1:c.-93-88A>C | NP_001365422.1:n.-93-88A>C |