Linked Data
ClinVar Variation Id:
2944577
ClinVar RCV Id:
RCV003808279
MyVariant Identifiers:
chr3:g.81627124G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81577973G>T , CM000665.2:g.81577973G>T | GRCh38 |
| NC_000003.11:g.81627124G>T , CM000665.1:g.81627124G>T | GRCh37 |
| NC_000003.10:g.81709814G>T | NCBI36 |
| NG_011810.1:g.188828C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429644.7:c.1570C>A MANE Select | ENSP00000410833.2:p.Arg524= | |
| ENST00000429644.6:c.1570C>A | ENSP00000410833.2:p.Arg524= | |
| ENST00000489715.1:c.1447C>A | ENSP00000419638.1:p.Arg483= | |
| NM_000158.3:c.1570C>A | NP_000149.3:p.Arg524= | |
| NM_000158.4:c.1570C>A MANE Select | NP_000149.4:p.Arg524= |