Linked Data
MyVariant Identifiers:
chr3:g.190122609A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190404820A>T , CM000665.2:g.190404820A>T | GRCh38 |
| NC_000003.11:g.190122609A>T , CM000665.1:g.190122609A>T | GRCh37 |
| NC_000003.10:g.191605303A>T | NCBI36 |
| NG_008149.1:g.21769A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264734.3:c.276A>T MANE Select | ENSP00000264734.3:p.Gly92= | |
| ENST00000456423.2:c.115-5083A>T | ENSP00000414136.2:n.115-5083A>T | |
| ENST00000264734.2:c.486A>T | ENSP00000264734.2:p.Gly162= | |
| ENST00000456423.1:c.325-5083A>T | ENSP00000414136.1:n.325-5083A>T | |
| ENST00000468220.1:n.468A>T | ||
| NM_006580.3:c.486A>T | NP_006571.1:p.Gly162= | |
| NM_001378492.1:c.276A>T | NP_001365421.1:p.Gly92= | |
| NM_001378493.1:c.276A>T | NP_001365422.1:p.Gly92= | |
| NM_006580.4:c.276A>T MANE Select | NP_006571.2:p.Gly92= |