Linked Data
ClinVar Variation Id:
3074932
ClinVar RCV Id:
RCV004015458
gnomAD v4:
3-46859590-G-A
MyVariant Identifiers:
chr3:g.46901080G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.46859590G>A , CM000665.2:g.46859590G>A | GRCh38 |
| NC_000003.11:g.46901080G>A , CM000665.1:g.46901080G>A | GRCh37 |
| NC_000003.10:g.46876084G>A | NCBI36 |
| NG_007555.2:g.27580C>T , LRG_395:g.27580C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000431168.2:c.366C>T | ENSP00000393455.2:p.Ser122= | |
| ENST00000292327.6:c.366C>T MANE Select | ENSP00000292327.4:p.Ser122= | |
| ENST00000653454.1:c.366C>T | ENSP00000499624.1:p.Ser122= | |
| ENST00000654597.1:c.366C>T | ENSP00000499406.1:p.Ser122= | |
| ENST00000655244.1:n.588C>T | ||
| ENST00000662933.1:c.366C>T | ENSP00000499577.1:p.Ser122= | |
| ENST00000664891.1:n.324C>T | ||
| ENST00000292327.4:c.366C>T | ENSP00000292327.4:p.Ser122= | |
| ENST00000395869.5:c.366C>T | ENSP00000379210.1:p.Ser122= | |
| NM_000258.2:c.366C>T , LRG_395t1:c.366C>T | NP_000249.1:p.Ser122= | |
| NM_000258.3:c.366C>T MANE Select | NP_000249.1:p.Ser122= |