Linked Data
MyVariant Identifiers:
chr13:g.48619923A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48045787A>T , CM000675.2:g.48045787A>T | GRCh38 |
| NC_000013.10:g.48619923A>T , CM000675.1:g.48619923A>T | GRCh37 |
| NC_000013.9:g.47517924A>T | NCBI36 |
| NG_047021.1:g.13221A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258662.3:c.483A>T MANE Select | ENSP00000258662.1:p.Gly161= | |
| ENST00000258662.2:c.483A>T | ENSP00000258662.1:p.Gly161= | |
| NM_018283.2:c.483A>T | NP_060753.1:p.Gly161= | |
| NM_018283.3:c.483A>T | NP_060753.1:p.Gly161= | |
| NR_136687.1:n.663A>T | ||
| NR_136688.1:n.663A>T | ||
| NM_018283.4:c.483A>T MANE Select | NP_060753.1:p.Gly161= | |
| NR_136687.2:n.504A>T | ||
| NR_136688.2:n.504A>T |