Linked Data
MyVariant Identifiers:
chr3:g.147131173T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.147413386T>C , CM000665.2:g.147413386T>C | GRCh38 |
| NC_000003.11:g.147131173T>C , CM000665.1:g.147131173T>C | GRCh37 |
| NC_000003.10:g.148613863T>C | NCBI36 |
| NG_015886.1:g.8993T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282928.5:c.1179T>C MANE Select | ENSP00000282928.4:p.Pro393= | |
| ENST00000282928.4:c.1179T>C | ENSP00000282928.4:p.Pro393= | |
| ENST00000472523.1:n.521+19444T>C | ||
| ENST00000488404.5:c.245T>C | ||
| NM_003412.3:c.1179T>C | NP_003403.2:p.Pro393= | |
| NM_003412.4:c.1179T>C MANE Select | NP_003403.2:p.Pro393= |