Linked Data
dbSNP Id:
rs1578278108
gnomAD v4:
3-129528787-T-G
MyVariant Identifiers:
chr3:g.129247630T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129528787T>G , CM000665.2:g.129528787T>G | GRCh38 |
| NC_000003.11:g.129247630T>G , CM000665.1:g.129247630T>G | GRCh37 |
| NC_000003.10:g.130730320T>G | NCBI36 |
| NG_009115.1:g.5149T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296271.4:c.54T>G MANE Select | ENSP00000296271.3:p.Gly18= | |
| ENST00000296271.3:c.54T>G | ENSP00000296271.3:p.Gly18= | |
| NM_000539.3:c.54T>G MANE Select | NP_000530.1:p.Gly18= |