Linked Data
MyVariant Identifiers:
chr1:g.196964855C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.196995725C>A , CM000663.2:g.196995725C>A | GRCh38 |
| NC_000001.10:g.196964855C>A , CM000663.1:g.196964855C>A | GRCh37 |
| NC_000001.9:g.195231478C>A | NCBI36 |
| NG_016365.1:g.23189C>A , LRG_227:g.23189C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699466.1:c.361C>A | ENSP00000514393.1:p.Arg121= | |
| ENST00000699467.1:n.685C>A | ||
| ENST00000699468.1:c.-24-389C>A | ENSP00000514394.1:n.-24-389C>A | |
| ENST00000256785.5:c.616C>A MANE Select | ENSP00000256785.4:p.Arg206= | |
| ENST00000256785.4:c.616C>A | ENSP00000256785.4:p.Arg206= | |
| NM_030787.3:c.616C>A , LRG_227t1:c.616C>A | NP_110414.1:p.Arg206= | |
| XM_011510020.1:c.625C>A | XP_011508322.1:p.Arg209= | |
| XM_011510020.2:c.625C>A | XP_011508322.1:p.Arg209= | |
| NM_030787.4:c.616C>A MANE Select | NP_110414.1:p.Arg206= |