Linked Data
MyVariant Identifiers:
chr1:g.160394922A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160425132A>T , CM000663.2:g.160425132A>T | GRCh38 |
| NC_000001.10:g.160394922A>T , CM000663.1:g.160394922A>T | GRCh37 |
| NC_000001.9:g.158661546A>T | NCBI36 |
| NG_023420.1:g.29559A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696602.1:c.1464A>T | ENSP00000512747.1:p.Arg488= | |
| ENST00000368061.3:c.1320A>T MANE Select | ENSP00000357040.2:p.Arg440= | |
| ENST00000368061.2:c.1320A>T | ENSP00000357040.2:p.Arg440= | |
| NM_020335.2:c.1320A>T | NP_065068.1:p.Arg440= | |
| XM_005245357.1:c.1320A>T | XP_005245414.1:p.Arg440= | |
| XM_011509804.1:c.1320A>T | XP_011508106.1:p.Arg440= | |
| NM_020335.3:c.1320A>T MANE Select | NP_065068.1:p.Arg440= |