Linked Data
MyVariant Identifiers:
chr5:g.145719428A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.146339865A>T , CM000667.2:g.146339865A>T | GRCh38 |
| NC_000005.9:g.145719428A>T , CM000667.1:g.145719428A>T | GRCh37 |
| NC_000005.8:g.145699621A>T | NCBI36 |
| NG_011885.1:g.5842A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646991.2:c.438A>T MANE Select | ENSP00000495718.1:p.Pro146= | |
| ENST00000230732.4:c.438A>T | ENSP00000230732.4:p.Pro146= | |
| NM_002700.2:c.438A>T | NP_002691.1:p.Pro146= | |
| NM_002700.3:c.438A>T MANE Select | NP_002691.1:p.Pro146= |