Linked Data
MyVariant Identifiers:
chr3:g.52258203C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.52224187C>T , CM000665.2:g.52224187C>T | GRCh38 |
| NC_000003.11:g.52258203C>T , CM000665.1:g.52258203C>T | GRCh37 |
| NC_000003.10:g.52233243C>T | NCBI36 |
| NG_033933.1:g.6977G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360658.3:c.129G>A MANE Select | ENSP00000353874.2:p.Val43= | |
| ENST00000360658.2:c.129G>A | ENSP00000353874.2:p.Val43= | |
| ENST00000478201.1:c.303G>A | ||
| ENST00000494383.1:c.589G>A | ||
| NM_017442.3:c.129G>A | NP_059138.1:p.Val43= | |
| NM_017442.4:c.129G>A MANE Select | NP_059138.1:p.Val43= |