Linked Data
MyVariant Identifiers:
chr3:g.52258190G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.52224174G>A , CM000665.2:g.52224174G>A | GRCh38 |
| NC_000003.11:g.52258190G>A , CM000665.1:g.52258190G>A | GRCh37 |
| NC_000003.10:g.52233230G>A | NCBI36 |
| NG_033933.1:g.6990C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360658.3:c.142C>T MANE Select | ENSP00000353874.2:p.Leu48= | |
| ENST00000360658.2:c.142C>T | ENSP00000353874.2:p.Leu48= | |
| ENST00000478201.1:c.316C>T | ||
| ENST00000494383.1:c.602C>T | ||
| NM_017442.3:c.142C>T | NP_059138.1:p.Leu48= | |
| NM_017442.4:c.142C>T MANE Select | NP_059138.1:p.Leu48= |