Linked Data
MyVariant Identifiers:
chr3:g.129249739T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129530896T>C , CM000665.2:g.129530896T>C | GRCh38 |
| NC_000003.11:g.129249739T>C , CM000665.1:g.129249739T>C | GRCh37 |
| NC_000003.10:g.130732429T>C | NCBI36 |
| NG_009115.1:g.7258T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296271.4:c.382T>C MANE Select | ENSP00000296271.3:p.Leu128= | |
| ENST00000296271.3:c.382T>C | ENSP00000296271.3:p.Leu128= | |
| NM_000539.3:c.382T>C MANE Select | NP_000530.1:p.Leu128= |