Linked Data
MyVariant Identifiers:
chr1:g.160109746A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160139956A>T , CM000663.2:g.160139956A>T | GRCh38 |
| NC_000001.10:g.160109746A>T , CM000663.1:g.160109746A>T | GRCh37 |
| NC_000001.9:g.158376370A>T | NCBI36 |
| NG_008014.1:g.29199A>T , LRG_6:g.29199A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361216.8:c.3006A>T MANE Select | ENSP00000354490.3:p.Arg1002= | |
| ENST00000361216.7:c.3006A>T | ENSP00000354490.3:p.Arg1002= | |
| ENST00000392233.7:c.2973A>T | ENSP00000376066.3:p.Arg991= | |
| ENST00000447527.1:c.2087A>T | ||
| ENST00000463989.1:n.342A>T | ||
| NM_000702.3:c.3006A>T | NP_000693.1:p.Arg1002= | |
| NM_000702.4:c.3006A>T MANE Select | NP_000693.1:p.Arg1002= |