Linked Data
MyVariant Identifiers:
chr5:g.145719404G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.146339841G>T , CM000667.2:g.146339841G>T | GRCh38 |
| NC_000005.9:g.145719404G>T , CM000667.1:g.145719404G>T | GRCh37 |
| NC_000005.8:g.145699597G>T | NCBI36 |
| NG_011885.1:g.5818G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646991.2:c.414G>T MANE Select | ENSP00000495718.1:p.Ser138= | |
| ENST00000230732.4:c.414G>T | ENSP00000230732.4:p.Ser138= | |
| NM_002700.2:c.414G>T | NP_002691.1:p.Ser138= | |
| NM_002700.3:c.414G>T MANE Select | NP_002691.1:p.Ser138= |